WO2021222587A1 - Protéines anti-cd26 et leurs utilisations - Google Patents

Protéines anti-cd26 et leurs utilisations Download PDF

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Publication number
WO2021222587A1
WO2021222587A1 PCT/US2021/029920 US2021029920W WO2021222587A1 WO 2021222587 A1 WO2021222587 A1 WO 2021222587A1 US 2021029920 W US2021029920 W US 2021029920W WO 2021222587 A1 WO2021222587 A1 WO 2021222587A1
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amino acids
seq
chain variable
variable domain
protein
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PCT/US2021/029920
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English (en)
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Hing C. Wong
Bai LIU
Lin KONG
Xiaoyun Zhu
Catherine SPANOUDIS
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HCW Biologics, Inc.
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Priority to AU2021262794A priority Critical patent/AU2021262794A1/en
Priority to CN202180043401.3A priority patent/CN115836087A/zh
Priority to EP21727042.0A priority patent/EP4143231A1/fr
Priority to US17/922,067 priority patent/US20230174666A1/en
Priority to JP2022566042A priority patent/JP2023525495A/ja
Priority to CA3181417A priority patent/CA3181417A1/fr
Publication of WO2021222587A1 publication Critical patent/WO2021222587A1/fr

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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K16/00—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
    • C07K16/18—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans
    • C07K16/28—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants
    • C07K16/2896—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants against molecules with a "CD"-designation, not provided for elsewhere
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K35/00—Medicinal preparations containing materials or reaction products thereof with undetermined constitution
    • A61K35/12—Materials from mammals; Compositions comprising non-specified tissues or cells; Compositions comprising non-embryonic stem cells; Genetically modified cells
    • A61K35/14—Blood; Artificial blood
    • A61K35/17—Lymphocytes; B-cells; T-cells; Natural killer cells; Interferon-activated or cytokine-activated lymphocytes
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K38/00—Medicinal preparations containing peptides
    • A61K38/16—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • A61K38/17—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
    • A61K38/177—Receptors; Cell surface antigens; Cell surface determinants
    • A61K38/1774—Immunoglobulin superfamily (e.g. CD2, CD4, CD8, ICAM molecules, B7 molecules, Fc-receptors, MHC-molecules)
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K39/00—Medicinal preparations containing antigens or antibodies
    • A61K39/0005—Vertebrate antigens
    • A61K39/0011—Cancer antigens
    • A61K39/001154—Enzymes
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
    • A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K16/00—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
    • C07K16/40—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against enzymes
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K39/00—Medicinal preparations containing antigens or antibodies
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K2317/00—Immunoglobulins specific features
    • C07K2317/20—Immunoglobulins specific features characterized by taxonomic origin
    • C07K2317/21—Immunoglobulins specific features characterized by taxonomic origin from primates, e.g. man
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K2317/00—Immunoglobulins specific features
    • C07K2317/20—Immunoglobulins specific features characterized by taxonomic origin
    • C07K2317/24—Immunoglobulins specific features characterized by taxonomic origin containing regions, domains or residues from different species, e.g. chimeric, humanized or veneered
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K2317/00—Immunoglobulins specific features
    • C07K2317/60—Immunoglobulins specific features characterized by non-natural combinations of immunoglobulin fragments
    • C07K2317/62—Immunoglobulins specific features characterized by non-natural combinations of immunoglobulin fragments comprising only variable region components
    • C07K2317/622—Single chain antibody (scFv)

Definitions

  • BACKGROUND CD26 (DPP4, also known as Dipeptidyl-peptidase-4, DDP4) is a transmembrane glycoprotein, anchored to the membrane by its signal peptide, that forms a homodimer or tetramer on the plasma membrane.
  • CD26 is an amino peptidase that primarily cleaves N- terminal dipeptides from peptides or small proteins (e.g., below 80-100 amino acid residues) with proline or alanine as the penultimate amino acid.
  • CD26 is expressed in numerous tissues including intestinal and renal brush border membranes, vascular endothelium, liver and pancreas, glandular epithelial cells, and by cells of the immune system (Gutschmidt et al., Histochemistry 73(2):285-304, 1982; Gorrell et al., Cell. Immunol.134(1):205-215, 1991; Tanaka et al., J. Immunol.
  • CD26 was also found to function as a binding site for the chemokine CXCR4 receptor, the T-cell differentiation antigen CD45, and the sodium- hydrogen exchanger-3 (Mentlein et al., Regul.
  • CD26 can be viewed as a multi- functional protein with a variety of actions which go beyond its role as a proteinase. Its role as a receptor or ligand for a variety of different molecules, either alone or in combination with its enzymatic activity, enable it to affect physiological processes such as the interaction between cells and the extracellular matrix involved in cell migration, activation, and proliferation. CD26 also plays a major role in glucose metabolism.
  • Incretin peptides such as gastric inhibitory polypeptide (GIP) and glucagon-like peptide (GLP-1) are responsible for the modulation of postprandial blood glucose by promoting insulin secretion from pancreatic ⁇ cells and via glucagon static effects. These peptides are rapidly inactivated by CD26 resulting in a short half-life. Besides incretin peptides, CD26 also cleaves a number of other proteins.
  • the physiologic targets include GLP1, GLP2, brain natriuretic peptide, peptide YY, stromal-cell-derived factor, erythropoietin, granulocyte colony- stimulating factor, and substance P.
  • Pharmacological targets include gastric-releasing peptide, growth-hormone-releasing factor, macrophage derived chemokine, eotaxin, IFN- ⁇ -induced protein-10, granulocyte-macrophage colony-stimulating factor, erythropoietin, IL-3, neuropeptide Y, B-type natriuretic peptide, and peptide YY (Mulvihill et al., Endocr. Rev.35(6):992-1019, 2014).
  • CD26 is known to modulate the functionality of chemokines, such as CXCR3, through post-translational cleavage of X- Pro or X-Ala motifs, which leads to amino-terminal dipeptide truncation of chemokines and altered biological functions (Broxmeyer et al., Stem Cells Dev.25(8):575-585, 2016).
  • CD26 also mediates amino-terminal cleavage of the chemokine CXCL10, limiting the migration of CXCR3 natural killer (NK) and T cells and diminution of anti-tumor immunity in preclinical models of melanoma and colorectal carcinoma (Barreira et al., Nat. Immunol.16(8):850-858, 2015).
  • CD26 exerts its physiological roles either via its enzymatic activity by regulating many peptides or via its interactions with a variety of binding partners. Consequently, altered expression, and/or activity of CD26 have been implicated in several pathological processes, including inflammation, viral infection, immune-mediated diseases, tumor growth, cellular senescence, and metabolic diseases (Mentlein et al., Regul.
  • CD26 is a cell-surface targetable protein for drug development to treat a variety of diseases including viral infections and aging-related pathologies SUMMARY
  • the anti-CD26 antigen-binding domain comprises: (a) a heavy chain variable domain comprising a CDR1 comprising SEQ ID NO: 1, a CDR2 comprising SEQ ID NO: 2, and a CDR3 comprising SEQ ID NO: 3, and a light chain variable domain comprising a CDR1 comprising SEQ ID NO: 4, a CDR2 comprising SEQ ID NO: 5, and a CDR3 comprising SEQ ID NO: 6; (b) a heavy chain variable domain comprising a CDR1 comprising SEQ ID NO: 7, a CDR2 comprising SEQ ID NO: 8, and a CDR3 comprising SEQ ID NO: 9, and a light chain variable domain comprising a CDR1 comprising SEQ ID NO: 10, a CDR2 comprising S
  • the antigen-binding domain comprises a heavy chain variable domain comprising a CDR1 comprising SEQ ID NO: 1, a CDR2 comprising SEQ ID NO: 2, and a CDR3 comprising SEQ ID NO: 3, and a light chain variable domain comprising a CDR1 comprising SEQ ID NO: 4, a CDR2 comprising SEQ ID NO: 5, and a CDR3 comprising SEQ ID NO: 6.
  • the heavy chain variable domain comprises a sequence that is at least 80% identical to SEQ ID NO: 61. In some embodiments, the heavy chain variable domain comprises a sequence that is at least 90% identical to SEQ ID NO: 61.
  • the heavy chain variable domain comprises a sequence that is at least 95% identical to SEQ ID NO: 61. In some embodiments, the light chain variable domain comprises a sequence that is at least 80% identical to SEQ ID NO: 62. In some embodiments, the light chain variable domain comprises a sequence that is at least 90% identical to SEQ ID NO: 62. In some embodiments, the light chain variable domain comprises a sequence that is at least 95% identical to SEQ ID NO: 62.
  • the antigen-binding domain comprises a heavy chain variable domain comprising a CDR1 comprising SEQ ID NO: 7, a CDR2 comprising SEQ ID NO: 8, and a CDR3 comprising SEQ ID NO: 9, and a light chain variable domain comprising a CDR1 comprising SEQ ID NO: 10, a CDR2 comprising SEQ ID NO: 11, and a CDR3 comprising SEQ ID NO: 12.
  • the heavy chain variable domain comprises a sequence that is at least 80% identical to SEQ ID NO: 63. In some embodiments, the heavy chain variable domain comprises a sequence that is at least 90% identical to SEQ ID NO: 63.
  • the heavy chain variable domain comprises a sequence that is at least 95% identical to SEQ ID NO: 63. In some embodiments, the light chain variable domain comprises a sequence that is at least 80% identical to SEQ ID NO: 64. In some embodiments, the light chain variable domain comprises a sequence that is at least 90% identical to SEQ ID NO: 64. In some embodiments, the light chain variable domain comprises a sequence that is at least 95% identical to SEQ ID NO: 64.
  • the antigen-binding domain comprises a heavy chain variable domain comprising a CDR1 comprising SEQ ID NO: 13, a CDR2 comprising SEQ ID NO: 14, and a CDR3 comprising SEQ ID NO: 15, and a light chain variable domain comprising a CDR1 comprising SEQ ID NO: 16, a CDR2 comprising SEQ ID NO: 17, and a CDR3 comprising SEQ ID NO: 18.
  • the heavy chain variable domain comprises a sequence that is at least 80% identical to SEQ ID NO: 65. In some embodiments, the heavy chain variable domain comprises a sequence that is at least 90% identical to SEQ ID NO: 65.
  • the heavy chain variable domain comprises a sequence that is at least 95% identical to SEQ ID NO: 65. In some embodiments, the light chain variable domain comprises a sequence that is at least 80% identical to SEQ ID NO: 66. In some embodiments, the light chain variable domain comprises a sequence that is at least 90% identical to SEQ ID NO: 66. In some embodiments, the light chain variable domain comprises a sequence that is at least 95% identical to SEQ ID NO: 66.
  • the antigen-binding domain comprises a heavy chain variable domain comprising a CDR1 comprising SEQ ID NO: 19, a CDR2 comprising SEQ ID NO: 20, and a CDR3 comprising SEQ ID NO: 21, and a light chain variable domain comprising a CDR1 comprising SEQ ID NO: 22, a CDR2 comprising SEQ ID NO: 23, and a CDR3 comprising SEQ ID NO: 24.
  • the heavy chain variable domain comprises a sequence that is at least 80% identical to SEQ ID NO: 67. In some embodiments, the heavy chain variable domain comprises a sequence that is at least 90% identical to SEQ ID NO: 67.
  • the heavy chain variable domain comprises a sequence that is at least 95% identical to SEQ ID NO: 67. In some embodiments, the light chain variable domain comprises a sequence that is at least 80% identical to SEQ ID NO: 68. In some embodiments, the light chain variable domain comprises a sequence that is at least 90% identical to SEQ ID NO: 68. In some embodiments, the light chain variable domain comprises a sequence that is at least 95% identical to SEQ ID NO: 68.
  • the antigen-binding domain comprises a heavy chain variable domain comprising a CDR1 comprising SEQ ID NO: 25, a CDR2 comprising SEQ ID NO: 26, and a CDR3 comprising SEQ ID NO: 27, and a light chain variable domain comprising a CDR1 comprising SEQ ID NO: 28, a CDR2 comprising SEQ ID NO: 29, and a CDR3 comprising SEQ ID NO: 30.
  • the heavy chain variable domain comprises a sequence that is at least 80% identical to SEQ ID NO: 69. In some embodiments, the heavy chain variable domain comprises a sequence that is at least 90% identical to SEQ ID NO: 69.
  • the heavy chain variable domain comprises a sequence that is at least 95% identical to SEQ ID NO: 69. In some embodiments, the light chain variable domain comprises a sequence that is at least 80% identical to SEQ ID NO: 70. In some embodiments, the light chain variable domain comprises a sequence that is at least 90% identical to SEQ ID NO: 70. In some embodiments, the light chain variable domain comprises a sequence that is at least 95% identical to SEQ ID NO: 70.
  • the antigen-binding domain comprises a heavy chain variable domain comprising a CDR1 comprising SEQ ID NO: 31, a CDR2 comprising SEQ ID NO: 32, and a CDR3 comprising SEQ ID NO: 33, and a light chain variable domain comprising a CDR1 comprising SEQ ID NO: 34, a CDR2 comprising SEQ ID NO: 35, and a CDR3 comprising SEQ ID NO: 36.
  • the heavy chain variable domain comprises a sequence that is at least 80% identical to SEQ ID NO: 71.
  • the heavy chain variable domain comprises a sequence that is at least 90% identical to SEQ ID NO: 71.
  • the heavy chain variable domain comprises a sequence that is at least 95% identical to SEQ ID NO: 71. In some embodiments, the light chain variable domain comprises a sequence that is at least 80% identical to SEQ ID NO: 72. In some embodiments, the light chain variable domain comprises a sequence that is at least 90% identical to SEQ ID NO: 72. In some embodiments, the light chain variable domain comprises a sequence that is at least 95% identical to SEQ ID NO: 72.
  • the antigen-binding domain comprises a heavy chain variable domain comprising a CDR1 comprising SEQ ID NO: 37, a CDR2 comprising SEQ ID NO: 38, and a CDR3 comprising SEQ ID NO: 39, and a light chain variable domain comprising a CDR1 comprising SEQ ID NO: 40, a CDR2 comprising SEQ ID NO: 41, and a CDR3 comprising SEQ ID NO: 42.
  • the heavy chain variable domain comprises a sequence that is at least 80% identical to SEQ ID NO: 73. In some embodiments, the heavy chain variable domain comprises a sequence that is at least 90% identical to SEQ ID NO: 73.
  • the heavy chain variable domain comprises a sequence that is at least 95% identical to SEQ ID NO: 73. In some embodiments, the light chain variable domain comprises a sequence that is at least 80% identical to SEQ ID NO: 74. In some embodiments, the light chain variable domain comprises a sequence that is at least 90% identical to SEQ ID NO: 74. In some embodiments, the light chain variable domain comprises a sequence that is at least 95% identical to SEQ ID NO: 74.
  • the antigen-binding domain comprises a heavy chain variable domain comprising a CDR1 comprising SEQ ID NO: 43, a CDR2 comprising SEQ ID NO: 44, and a CDR3 comprising SEQ ID NO: 45, and a light chain variable domain comprising a CDR1 comprising SEQ ID NO: 46, a CDR2 comprising SEQ ID NO: 47, and a CDR3 comprising SEQ ID NO: 48.
  • the heavy chain variable domain comprises a sequence that is at least 80% identical to SEQ ID NO: 75. In some embodiments, the heavy chain variable domain comprises a sequence that is at least 90% identical to SEQ ID NO: 75.
  • the heavy chain variable domain comprises a sequence that is at least 95% identical to SEQ ID NO: 75. In some embodiments, the light chain variable domain comprises a sequence that is at least 80% identical to SEQ ID NO: 76. In some embodiments, the light chain variable domain comprises a sequence that is at least 90% identical to SEQ ID NO: 76. In some embodiments, the light chain variable domain comprises a sequence that is at least 95% identical to SEQ ID NO: 76.
  • the antigen-binding domain comprises a heavy chain variable domain comprising a CDR1 comprising SEQ ID NO: 49, a CDR2 comprising SEQ ID NO: 50, and a CDR3 comprising SEQ ID NO: 51, and a light chain variable domain comprising a CDR1 comprising SEQ ID NO: 52, a CDR2 comprising SEQ ID NO: 53, and a CDR3 comprising SEQ ID NO: 54.
  • the heavy chain variable domain comprises a sequence that is at least 80% identical to SEQ ID NO: 77. In some embodiments, the heavy chain variable domain comprises a sequence that is at least 90% identical to SEQ ID NO: 77.
  • the heavy chain variable domain comprises a sequence that is at least 95% identical to SEQ ID NO: 77. In some embodiments, the light chain variable domain comprises a sequence that is at least 80% identical to SEQ ID NO: 78. In some embodiments, the light chain variable domain comprises a sequence that is at least 90% identical to SEQ ID NO: 78. In some embodiments, the light chain variable domain comprises a sequence that is at least 95% identical to SEQ ID NO: 78.
  • the antigen-binding domain comprises a heavy chain variable domain comprising a CDR1 comprising SEQ ID NO: 55, a CDR2 comprising SEQ ID NO: 56, and a CDR3 comprising SEQ ID NO: 57, and a light chain variable domain comprising a CDR1 comprising SEQ ID NO: 58, a CDR2 comprising SEQ ID NO: 59, and a CDR3 comprising SEQ ID NO: 60.
  • the heavy chain variable domain comprises a sequence that is at least 80% identical to SEQ ID NO: 79.
  • the heavy chain variable domain comprises a sequence that is at least 90% identical to SEQ ID NO: 79.
  • the heavy chain variable domain comprises a sequence that is at least 95% identical to SEQ ID NO: 79. In some embodiments, the light chain variable domain comprises a sequence that is at least 80% identical to SEQ ID NO: 80. In some embodiments, the light chain variable domain comprises a sequence that is at least 90% identical to SEQ ID NO: 80. In some embodiments, the light chain variable domain comprises a sequence that is at least 95% identical to SEQ ID NO: 80. In some embodiments, the protein is a multi-chain protein. In some embodiments, the protein is a single-chain protein. In some embodiments, the protein is an antibody or an antigen-binding antibody fragment.
  • the antibody is an IgG1 antibody, an IgG2 antibody, an IgG3 antibody, or an IgG4 antibody. In some embodiments, the antibody is humanized. In some embodiments, the antibody is human. In some embodiments, the protein is a scFv. In some embodiments, the protein is a chimeric antigen receptor (CAR). Also provided herein are pharmaceutical compositions comprising any one of the proteins described herein and a pharmaceutically acceptable carrier. Also provided herein are kits comprising any one of the pharmaceutical compositions described herein. Also provided herein are nucleic acids encoding any one of the proteins described herein. Also provided herein are vectors comprising any one of the nucleic acids described herein.
  • kits comprising any one of the pharmaceutical compositions described herein.
  • cells comprising any one of the nucleic acids described herein or any one of the vectors described herein.
  • the cell is an immune cell.
  • the immune cell is a T cell, a B cell, or a natural killer (NK) cell.
  • the immune cell is a regulatory T (Treg) cell.
  • the immune cell is an autologous cell.
  • the immune cell is an allogeneic cell.
  • kits comprising any one of the pharmaceutical compositions described herein.
  • methods of treating an age-related disease or an inflammatory disease in a subject that include administering to the subject a therapeutically effective amount of any one of the proteins described herein or any one of the pharmaceutical compositions described herein.
  • methods of treating an aging- related disease or an inflammatory disease in a subject that include administering to the subject a therapeutically effective amount of any one of the nucleic acids described herein, any one of the vectors described herein, or any one of the pharmaceutical compositions described herein.
  • the aging-related disease is inflamm-aging related.
  • the subject is further administered (i) a therapeutically effective amount of an NK cell activating agent and/or an NK cell and/or a monoclonal antibody; and/or (ii) a therapeutically effective amount of a Treg cell activating agent and/or a Treg cell and/or a monoclonal antibody and/or an advanced glycation end product (AGE) inhibitor.
  • AGE advanced glycation end product
  • the method comprises administering a therapeutically effective amount of an NK cell to the subject.
  • the NK cell is an autologous, haploidentical or allogeneic NK cell isolated from peripheral blood, umbilical cord blood, or isolated and differentiated from iPSC.
  • the method further comprises: isolating the NK cell from the subject; culturing the isolated NK cell in a liquid culture medium under conditions sufficient to induce or increase proliferation of the NK cell, wherein following the isolating and culturing steps, the NK cell is administered to the subject.
  • the liquid culture medium comprises a multi-chain chimeric polypeptide.
  • the NK cell comprises a chimeric antigen receptor.
  • the protein is any one of the chimeric antigen receptors described herein.
  • the method comprises administering a therapeutically effective amount of an NK cell activating agent and/or monoclonal antibody to the subject.
  • the NK cell activating agent is one or more multi-chain chimeric polypeptide(s).
  • the monoclonal antibody is any one of the anti-tissue factor antibodies or antibodies described herein.
  • the NK cell activating agent comprises one or more multi-chain chimeric polypeptide(s) and the monoclonal antibody comprises one or more of any one of the anti-tissue factor antibodies and/or antibodies described herein.
  • the method comprises administering a therapeutically effective amount of a Treg cell to the subject.
  • the Treg cell is an autologous Treg cell, a haploidentical Treg cell, or an allogeneic Treg cell isolated from peripheral blood or umbilical cord blood.
  • the method further comprises: isolating the Treg cell from the subject; culturing the isolated Treg cell in a liquid culture medium under conditions sufficient to induce or increase proliferation of the Treg cell, wherein following the isolating and culturing steps, the Treg cell is administered to the subject.
  • the liquid culture medium comprises one or more single-chain chimeric polypeptide(s).
  • the Treg cell comprises a chimeric antigen receptor.
  • the chimeric antigen receptor comprises an extracellular domain that binds specifically to tissue factor, CD26 (e.g., any of the anti-CD26 antigen-binding domains described herein), or CD36.
  • the method comprises administering a therapeutically effective amount of a Treg cell activating agent and/or monoclonal antibody and/or AGE inhibitor to the subject.
  • the Treg cell activating agent is one or more single-chain chimeric polypeptide(s).
  • the monoclonal antibody is one or both of an anti-tissue factor antibody, an anti-CD26 antibody (e.g., any of the anti- CD26 antibodies described herein), and/or an anti-CD36 antibody.
  • the AGE inhibitor is a soluble RAGE trap.
  • the Treg cell activating agent comprises one or more single-chain chimeric polypeptide(s)
  • the monoclonal antibody comprises one or more of an anti-tissue factor antibody, an anti- CD26 antibody (e.g., any of the anti-CD26 antibodies described herein), and/or an anti- CD36 antibody
  • the AGE inhibitor comprises one or more soluble RAGE trap.
  • the multi-chain chimeric polypeptide comprises: (a) a first chimeric polypeptide comprising: (i) a first target-binding domain; (ii) a soluble tissue factor domain; and (iii) a first domain of a pair of affinity domains; (b) a second chimeric polypeptide comprising: (i) a second domain of a pair of affinity domains; and (ii) a second target-binding domain, wherein the first chimeric polypeptide and the second chimeric polypeptide associate through the binding of the first domain and the second domain of the pair of affinity domains.
  • the single-chain chimeric polypeptide comprises: (i) a first target-binding domain; (ii) a soluble tissue factor domain; and (iii) a second target- binding domain.
  • the aging-related disorder is selected from the group of: Alzheimer’s disease, aneurysm, cystic fibrosis, fibrosis in pancreatitis, glaucoma, hypertension, idiopathic pulmonary fibrosis, inflammatory bowel disease, intervertebral disc degeneration, macular degeneration, osteoarthritis, type 2 diabetes mellitus, adipose atrophy, lipodystrophy, atherosclerosis, cataracts, COPD, idiopathic pulmonary fibrosis, kidney transplant failure, liver fibrosis, loss of bone mass, myocardial infarction, sarcopenia, wound healing, alopecia, cardiomyocyte hypertrophy, osteoarthritis, Parkinson’s disease, age-associated loss of lung
  • the inflammatory disease is selected from the group of: rheumatoid arthritis, inflammatory bowel disease, lupus erythematosus, lupus nephritis, diabetic nephropathy, CNS injury, Alzheimer’s disease, Parkinson’s disease, amyotrophic lateral sclerosis, Crohn’s disease, multiple sclerosis, Guillain-Barre syndrome, psoriasis, Grave’s disease, ulcerative colitis, nonalcoholic steatohepatitis, and mood disorders.
  • the age-related disease is a cancer selected from the group of: solid tumor, hematological tumor, sarcoma, osteosarcoma, glioblastoma, neuroblastoma, melanoma, rhabdomyosarcoma, Ewing sarcoma, osteosarcoma, B-cell neoplasms, multiple myeloma, B-cell lymphoma, B-cell non-Hodgkin’s lymphoma, Hodgkin’s lymphoma, chronic lymphocytic leukemia (CLL), acute myeloid leukemia (AML), chronic myeloid leukemia (CML), acute lymphocytic leukemia (ALL), myelodysplastic syndromes (MDS), cutaneous T-cell lymphoma, retinoblastoma, stomach cancer, urothelial carcinoma, lung cancer, renal cell carcinoma, gastric and esophageal cancer, pancreatic cancer, prostate cancer, breast cancer, breast cancer,
  • an “antigen-binding domain” is one or more protein domain(s) (e.g., formed from amino acids from a single polypeptide or formed from amino acids from two or more polypeptides (e.g., the same or different polypeptides) that is capable of specifically binding to an antigen.
  • an antigen-binding domain can bind to an antigen or epitope with specificity and affinity similar to that of naturally-occurring antibodies.
  • the antigen-binding domain can be an antibody or a fragment thereof.
  • an antigen-binding domain can include an alternative scaffold. Non-limiting examples of antigen-binding domains are described herein. Additional examples of antigen-binding domains are known in the art.
  • antibody is used herein in its broadest sense and includes certain types of immunoglobulin molecules that include one or more antigen-binding domains that specifically bind to an antigen or epitope.
  • An antibody specifically includes, e.g., intact antibodies (e.g., intact immunoglobulins, e.g., human IgG (e.g., human IgG1, human IgG2, human IgG3, human IgG4)), antibody fragments, and multi-specific antibodies.
  • an antigen-binding domain is an antigen-binding domain formed by a VH -VL dimer. Additional examples of an antibody are described herein. Additional examples of an antibody are known in the art.
  • affinity refers to the strength of the sum total of non-covalent interactions between an antigen-binding site and its binding partner (e.g., an antigen or epitope). Unless indicated otherwise, as used herein, “affinity” refers to intrinsic binding affinity, which reflects a 1:1 interaction between members of an antigen-binding domain and an antigen or epitope.
  • the affinity of a molecule X for its partner Y can be represented by the dissociation equilibrium constant (K D ). The kinetic components that contribute to the dissociation equilibrium constant are described in more detail below. Affinity can be measured by common methods known in the art, including those described herein.
  • Affinity can be determined, for example, using surface plasmon resonance (SPR) technology (e.g., BIACORE®) or biolayer interferometry (e.g., FORTEBIO®). Additional methods for determining the affinity for an antigen-binding domain and its corresponding antigen or epitope are known in the art.
  • SPR surface plasmon resonance
  • FORTEBIO® biolayer interferometry
  • the term “pair of affinity domains” is two different protein domain(s) that bind specifically to each other with a KD of less than of less than 1 x 10 -7 M (e.g., less than 1 x 10 -8 M, less than 1 x 10 -9 M, less than 1 x 10 -10 M, or less than 1 x 10 -11 M).
  • a pair of affinity domains can be a pair of naturally-occurring proteins. In some embodiments, a pair of affinity domains can be a pair of synthetic proteins. Non- limiting examples of pairs of affinity domains are described herein.
  • the term “epitope” means a portion of an antigen that specifically binds to an antigen-binding domain. Epitopes can, e.g., consist of surface-accessible amino acid residues and/or sugar side chains and may have specific three-dimensional structural characteristics, as well as specific charge characteristics. Conformational and non- conformational epitopes are distinguished in that the binding to the former but not the latter may be lost in the presence of denaturing solvents.
  • An epitope may comprise amino acid residues that are directly involved in the binding, and other amino acid residues, which are not directly involved in the binding.
  • Methods for identifying an epitope to which an antigen-binding domain binds are known in the art.
  • the term “treatment” means to ameliorate at least one symptom of a disorder.
  • the disorder being treated is cancer and to ameliorate at least one symptom of cancer includes reducing aberrant proliferation, gene expression, signaling, translation, and/or secretion of factors.
  • the methods of treatment include administering a therapeutically effective amount of composition that reduces at least one symptom of a disorder to a subject who is in need of, or who has been determined to be in need of such treatment.
  • Figure 1 shows ELISA binding analysis of selected scFv clones, where a plate of scFv clones were tested and their binding to CD26, Fc, and proA/L were tested, and DNA was prepared for scFv constructs then sent for DNA sequencing to determine LC/HC variable domain sequences.
  • Figure 2 shows sequence analysis of five unique scFv binding clones, where the unique clones were identified and sequencing results indicate that their LC and HC variable domains are intact and the sequences of CDR-L1, CDR-L2, CDR-L3, CDR-H1, CDR-H2, and CDR-H3 are unique from each other.
  • Figure 3 shows the binding of scFv supernatants to CD26 with serial dilution of scFv supernatants.
  • Figure 4 shows binding of scFvs with CD26 corrected for concentration, where the concentration of the scFvs was determined and the ELISA binding data was corrected for concentration.
  • Figure 5 shows the screening of CD26-binding scFvs, where clone CD26-03G and CD26-04E are shown in circled spots.
  • Figure 6 shows screening of CD26-binding scFvs in a YCM screen, where scFv clones CD26-01F, CD26-01G, and CD26-07H are shown in circled spots.
  • Figure 7 shows the sequences of selected scFvs.
  • Figure 8 shows human CD26-binding activity of anti-CD26 monoclonal antibodies.
  • Anti-CD26 IgG1kappa monoclonal antibodies were constructed based on the selected scFv sequences.
  • the CD26-binding of purified anti-CD26 monoclonal antibodies was determined with ELISA using (A) human CD26-Fc fusion protein-coated or (B) goat anti-human IgG-coated 96-well Maxisorp plates. The plates were blocked with blocking buffer. Purified anti-CD26 monoclonal antibodies were diluted in blocking buffer and added in the wells of CD26-Fc or goat anti-human IgG-coated plates.
  • the anti-CD26 monoclonal antibodies were probed with goat anti-human kappa-HRP/ABTS and read by an ELISA plate reader at 405 nM.
  • the results show that CD26Ab-01D and CD26Ab-04A are able to bind to CD26 and CD26Ab-01D has a better binding activity than CD26Ab-04A.
  • CD26Ab-12D and CD26Ab-03B have weak CD26-binding activity.
  • CD26Ab-10B has no significant CD26-binding activity.
  • Figure 9 shows human CD26-binding activity of anti-CD26 monoclonal antibodies.
  • Human CD26-transfected CHO cells were stained with (A) five different anti-CD26 monoclonal antibodies at 50 nM or (B) five different biotinylated anti-CD26 antibodies at 1 ⁇ g/test (26Ab-10B had very low production and was not biotinylated) and then probed using goat anti-human IgG-PE for unbiotinylated antibodies or using streptavidin-PE for the biotinylated antibodies.
  • the data was analyzed by BD FACSCelesta with BD FACSDiva Software.
  • Anti-tissue factor antibody (anti-TF Ab) was used as a negative control and PE-conjugated anti-CD26 (BioLegend) was used as a positive control.
  • FIG. 10 shows ADCC activity of different anti-CD26 monoclonal antibodies.
  • Human CD26-transfected CHO cells (CHO26) were labeled with CellTrace Violet and used as target cells, and fresh human NK cells (left: donor-1 and right: donor-2) were used as effector cells.
  • the effector cells were plated with violet-labelled target cells at the indicated effector:target (E:T) ratios with 26Ab-01D or 26Ab-04A at a 5 nM concentration.
  • Anti-tissue factor antibody (anti-TF Ab) was used as a control.
  • Target cell inhibition (%) was calculated using a formula: (1-[viable CHO26 cell number in experimental sample/viable CHO26 cell number in the sample without splenocytes]) x 100 on day 2 as assessed by flow cytometry and represents anti-CD26 antibody-mediated ADCC.
  • the results show CD26Ab-01D- and CD26Ab-04A-dependent and NK cell- mediated cytotoxicity against CD26-positive CHO cells.
  • Figure 11 shows interaction of human CD26 and adenosine deaminase (ADA). Human CD26-Fc fusion protein was used to coat 96-well Maxisorp plate. The plate was blocked with blocking buffer.
  • FIG. 12 is a schematic of a nucleic acid encoding an anti-CD26 CAR in a lentiviral vector.
  • Figure 13 is a set of images showing total Treg cells and anti-CD26 CAR Treg cells stimulated with the specific antigen (CD26/beads), non-specific antigen (TF/beads), or TCR (CD3/CD28/beads) for 3 days.
  • Figure 14 is a graph showing the fold-expansion of anti-CD26 CAR Treg cells after three days of stimulation with the specific antigen (CD26/beads), non-specific antigen (TF/beads), or TCR (CD3/CD28/beads).
  • Figure 15 is a set of fluorescence-assisted cell sorting (FACS) data showing the staining of anti-CD26 CAR Treg cells with CD26-Fc or tissue factor (TF).
  • FACS fluorescence-assisted cell sorting
  • Figure 16 is a graph showing cell marker expression in anti-CD26 CAR Treg cells and un-transduced Treg cells.
  • Figure 17 is a graph of the suppression activity of anti-CD26 CAR Treg cells and un-transduced Treg cells.
  • Figure 18 is a graph showing the suppression of IFNg production by Tresp cells with anti-CD26 CAR Treg cells or untransducted Treg cells.
  • Figure 19 is a graph showing the IL-10 production by anti-CD26 CAR Treg cells and untransduced Treg cells.
  • CD26 CD26 (DPP4, also known as Dipeptidyl-peptidase-4, DDP4) is a transmembrane glycoprotein, anchored to the membrane by its signal peptide, that forms a homodimer or tetramer on the plasma membrane.
  • CD26 is an amino peptidase that primarily cleaves N- terminal dipeptides from peptides or small proteins (below 80-100 amino acid residues) with proline or alanine as the penultimate amino acid. Protein substrates with glycine, serine, valine, or leucine can also be cleaved but at a slower rate. The enzyme is unable to cleave substrates with proline at position three.
  • CD26 is expressed in numerous tissues including intestinal and renal brush border membranes, vascular endothelium, liver and pancreas, glandular epithelial cells, and by cells of the immune system (Gutschmidt et al., Histochemistry 73(2):285-304, 1981; Gorrell et al., Cell Immunol.134(1):205-215, 1991; Tanaka et al., J. Immunol. 149(2):481-486, 1992; Abbott et al., Immunogenetics 40(5):331-338, 1994; Buhling et al., Immunol. Lett.45(1-2):47-51, 1995; Dikov et al., Cell. Mol.
  • CD26 The primary structure of CD26 consists of a six-amino acid cytoplasmic domain, a 22-amino acid transmembrane domain, and a 738- amino acid extracellular portion.
  • the extracellular portion is comprised of the C-terminal catalytic region with the catalytic active site triad Ser 630 , Asp 708 , and His 740 , a cysteine- rich area, and a large glycosylation-rich region linked by a flexible stalk to the transmembrane segment (Klemann et al., Clin. Exp. Immunol.185(1):1-21, 2016).
  • the crystal structure of human CD26 reveals two domains: an eight-bladed propeller and an ⁇ / ⁇ -hydrolase domain (Engel et al., Proc. Natl. Acad. Sci. U.S.A.100(9):5063-5068, 2003).
  • the propeller is open and consists of subdomains made up of blades II-V and VI- VIII for the glycosylation-rich and cysteine-rich regions, respectively.
  • Adenosine deaminase (ADA) and cavelolin-1 bind to the glycosylation-rich domain of human CD26, and collagen, fibronectin, plasminogen, and streptokinase bind to the cysteine-rich region (Klemann et al., Clin. Exp. Immunol.185(1):1-21, 2016).
  • CD26 substrate neuropeptide Y was found to enter CD26 at the side opening (Aertgeerts et al., Protein Sci.13(2):412-421, 2004). CD26 was also found to function as binding sites for the chemokine CXCR4 receptor, the T-cell differentiation antigen CD45, and the sodium-hydrogen exchanger-3 (Mentlein et al., Regul. Pept.85(1):9-24, 1999; Lambeir et al., Crit. Rev. Clin. Lab. Sci.40(3):209-294, 2003).
  • CD26 can be viewed as a multi-functional protein with a variety of actions which go beyond its role as a proteinase. Its role as a receptor or ligand for a variety of different molecules, either alone or in combination with its enzymatic activity, enable it to affect physiological processes, such as the interaction between cells and the extracellular matrix involved in cell migration, activation, and proliferation.
  • CD26 plays a major role in glucose metabolism. Incretin peptides, such as gastric inhibitory polypeptide (GIP) and glucagon-like peptide (GLP-1), are responsible for the modulation of postprandial blood glucose by promoting insulin secretion from pancreatic ⁇ cells and via glucagon static effects.
  • GIP gastric inhibitory polypeptide
  • GLP-1 glucagon-like peptide
  • CD26 -/- mice are protected from the development of diet- induced obesity and demonstrate improved postprandial glucose control due to the prolonged half-life of the incretin peptides.
  • CD26 -/- mice also demonstrate improved insulin sensitivity, reduced pancreatic islet hypertrophy, and protection against streptozotocin-induced ⁇ cell loss and hyperglycemia (Marguet et al., Proc. Natl. Acad. Sci. U.S.A.97(12):6874-6879, 2000; Conarello et al., Proc. Natl. Acad. Sci. U.S.A.
  • CD26 inhibitors approved by the US FDA as antidiabetic drugs, such as sitagliptin, saxagliptin, linagliptin, vildagliptin, and alogliptin. Most clinical trials with CD26 inhibitors show approximately a 0.6-0.8% lowering of HbA1C in patients with a baseline level around 8% (Inzucchi et al., Circulation 117(4):574-584, 2008).
  • the physiologic targets include GLP1, GLP2, brain natriuretic peptide, peptide YY, stromal- cell-derived factor, erythropoietin, granulocyte colony-stimulating factor, and substance P.
  • Pharmacological targets include gastric-releasing peptide, growth-hormone-releasing factor, macrophage derived chemokine, eotaxin, IFN- ⁇ -induced protein-10, granulocyte- macrophage colony-stimulating factor, erythropoietin, IL-3, neuropeptide Y, B-type natriuretic peptide, and peptide YY (Mulvihill et al., Endocr.
  • CD26 is known to modulate the functionality of chemokines, such as CXCR3, through post-translational cleavage of X-Pro or X-Ala motifs, which leads to amino- terminal dipeptide truncation of chemokines and altered biological function (Broxmeyer et al., Stem Cells Dev.25(8):575-585, 2016). CD26 also mediates amino-terminal cleavage of the chemokine CXCL10, limiting the migration of CXCR3 natural killer (NK) and T cells and diminution of anti-tumor immunity in preclinical models of melanoma and colorectal carcinoma (Barreira da Silva et al., Nat.
  • CD26 interacts also with a range of ligands. By interacting with these ligands, CD26 plays a role in a variety of processes such as enhancing T-cell activation and functional modulation of antigen presenting cells (APCs).
  • APCs antigen presenting cells
  • CD26 is able to trigger direct T cell activation and proliferation via CARMA1-mediated nuclear factor NF- ⁇ B in T cells (Ohnuma et al., J. Immunol.167(12):6745-6755, 2001; Ohnuma et al., Proc. Natl. Acad. Sci. U.S.A.101(39):14186-14191, 2004).
  • CD26 on T cells interacts directly with APCs via caveolin-1. Upon linkage, Tollip and interleukin-1-receptor associated kinase 1 (1RAK-1) disengage from caveolin-1 leading to subsequent 1RAK-1 phosphorylation (Ohnuma et al., Mol. Cell.
  • Interaction between CD26 and ADA also facilitate T-cell activation by providing a suitable microenvironment for T-cell proliferation.
  • Extracellular ATP or ADP is initially converted to AMP by CD39 and CD73 to produce adenosine (Deaglio et al., J. Exp. Med.204(6):1257-1265, 2007).
  • Adenosine is then processed by ADA and converted to inosine (Resta et al., Immunol. Rev.161:95-109, 1998).
  • Adenosine has multiple physiological effects both within the central nervous system, immune system, and on peripheral tissues that are mediated by the G-protein coupled adenosine receptors identified as A1, A2A, A2B, and A3 (Borea et al., Physiol. Rev.98(3):1591-1625, 2018).
  • ADA G-protein coupled adenosine receptors identified as A1, A2A, A2B, and A3
  • Jurkat cells expressing a CD26 mutant devoid of ADA binding activity are sensitive to adenosine- mediated inhibition of T-cell proliferation (Dong et al., J. Immunol.159(12):6070-6076, 1997).
  • Cells expressing ADA and CD26 on the surface are much more resistant to the inhibitory effect of adenosine (Dong et al., J. Immunol.156(4):1349-1355, 1996; Dong et al., J. Immunol.159(12):6070-6076, 1997; Zhong et al., Diabetes 62(1):149-157, 2013).
  • ADA co-localizing with adenosine receptors on dendritic cells and interacts with CD26 that is expressed on lymphocytes (Moreno et al., Front. Pharmacol.9:106, 2018).
  • This capacity of ADA functions as a costimulatory signal that potentiates T-cell activation and induces the production of the T-helper cell (Th1) pro- inflammatory cytokines.
  • CD26 binds multiple components of extracellular matrix such as collagen, fibronectin, and HIV-1 Tat protein (Loster et al., Biochem. Biophys. Res. Comm. 217(1):341-348, 1995; Zhong et al., Diabetes 62(1):149-157, 2013).
  • CD26 A humanized monoclonal antibody to CD26 showed promising antitumor efficacy and was well tolerated in a recently reported Phase I clinical study in patients with advanced malignant pleural mesothelioma (Takeda et al., Lung Cancer 137:64-70, 2019). CD26 is also implicated in cellular senescence, a hallmark of aging. Senescent cell accumulation in tissues is strongly linked to age-associated pathologies (Childs et al., Nat. Rev. Drug Discov.16(10):718-735, 2017; Kirkland et al., EBioMedicine 21:21-28, 2017).
  • CD26 was upregulated on the surface of human senescent diploid fibroblasts (Kim et al., Genes Dev.31(15):1529-1534, 2017). Increased CD26 expression on senescent, but not dividing, fibroblasts sensitized the fibroblasts to NK-mediated ADCC by anti-CD26 antibody (Kim et al., Genes Dev. 31(15):1529-1534, 2017). Senescence is a form of irreversible growth arrest accompanied by phenotypic changes, resistance to apoptosis and activation of damage-sensing signaling pathways.
  • Senescence was first described in cultured human fibroblast cells that lost their ability to proliferate, reaching permanent arrest after about 50 population doublings (referred to as the Hayflick limit). Senescence is considered a stress response that can be induced by a wide range of intrinsic and extrinsic insults, including oxidative and genotoxic stress, DNA damage, telomere attrition, oncogenic activation, mitochondrial dysfunction, or chemotherapeutic agents. Senescent cells remain metabolically active and can influence the tissue hemostasis, disease and aging through their secretory phenotype. Senescence is considered as a physiologic process and is important in promoting wound healing, tissue homeostasis, regeneration, and fibrosis regulation.
  • transient induction of senescent cells is observed during would healing and contributes to wound resolution.
  • Perhaps one of the most important roles of senescence is its role in tumor suppression.
  • the senescent phenotype also can trigger chronic inflammatory responses and consequently augment chronic inflammatory conditions to promote tumor growth.
  • the connection between senescence and aging was initially based on observations that senescent cells accumulate in aged tissue.
  • the use of transgenic models has enabled the detection of senescent cells systematically in many age-related pathologies. Strategies to selectively eliminate senescent cells have demonstrated that senescent cells can indeed play a causal role in aging and related pathologies.
  • Senescent cells display important and unique properties which include changes in morphology, chromatin organization, gene expression, and metabolism.
  • biochemical and functional properties associated with cellular senescence such as (i) increased expression of p16 and p21, inhibitors of cyclin-dependent kinases, (ii) presence of senescence-associated ⁇ -galactosidase, a marker of lysosomal activity, (iii) appearance of senescence-associated heterochromatin foci and downregulation of lamin B1 levels, (iv) resistance to apoptosis caused by an increased expression of anti-apoptotic BCL-family protein, and (v) upregulation of CD26 (DPP4), CD36 (Scavenger receptor), forkhead box 4 (FOXO4), and secretory carrier membrane protein 4 (SCAMP4).
  • Senescent cells also express an inflammatory signature, the so-called senescence- associated secretory phenotype (SASP).
  • SASP senescence- associated secretory phenotype
  • IL-6 IL-6
  • TGF- ⁇ growth factors
  • CCL-2 chemokines
  • MMP-3 matrix metalloproteinases
  • SASP factors can contribute to tumor suppression by triggering senescence surveillance, an immune-mediated clearance of senescent cells.
  • DNA damage results in: (1) high deposition of ⁇ H2Ax (histone coding gene) and 53BP1 (involved in DNA damage response) in chromatin: this leads to activation of a kinase cascade eventually resulting in p53 activation, and (2) activation of p16INK4a and ARF (both encoded by CDKN2A) and P15INK4b (encoded by CDKN2B): p53 induces transcription of cyclin-dependent kinase inhibitor (p21) and along with both p16INK4a and p15INK4b block genes for cell cycle progression (CDK4 and CDK6).
  • ⁇ H2Ax histone coding gene
  • 53BP1 involved in DNA damage response
  • NK cells such as IL-15 and CCL2
  • macrophages such as CFS-1 and CCL2
  • NK cells such as IL-15 and CCL2
  • SASP factors that function as chemoattractants mainly for .
  • NK cells such as IL-15 and CCL2
  • macrophages such as CFS-1 and CCL2
  • innate immune cells mediate the immunosurveillance mechanism for eliminating stressed cells.
  • Senescent cells usually up-regulate the NK-cell activating receptor NKG2D and DNAM-1 ligands, which belong to a family of stress-inducible ligands: an important component of the frontline immune defense against infectious diseases and malignancies.
  • NK cells can then specifically induce the death of senescent cells through their cytolytic machinery.
  • NK cells A role for NK cells in the immune surveillance of senescent cells has been pointed out in liver fibrosis (Sagiv et al., Oncogene 32(15):1971-1977, 2013), hepatocellular carcinoma (Iannello et al., J. Exp. Med.210(10):2057-2069, 2013), multiple myeloma (Soriani et al., Blood 113(15):3503-3511, 2009), and glioma cells stressed by dysfunction of the mevalonate pathway (Ciaglia et al., Int. J. Cancer 142(1):176-190, 2018). Endometrial cells undergo acute cellular senescence and do not differentiate into decidual cells.
  • the differentiated decidual cells secrete IL-15 and thereby recruit uterine NK cells to target and eliminate the undifferentiated senescent cells thus helping to re-model and rejuvenate the endometrium (Brighton et al., Elife 6:e31274, 2017).
  • p53-expressing senescent liver satellite cells skewed the polarization of resident Kupfer macrophages and freshly infiltrated macrophages toward the pro-inflammatory M1 phenotype, which display senolytic activity.
  • F4/80 + macrophages have been shown to play a key role in the clearance of mouse uterine senescent cells to maintain postpartum uterine function.
  • Senescent cells recruit NK cells by mainly upregulating ligands to NKG2D (expressed on NK cells), chemokines, and other SASP factors.
  • NK cells mainly upregulating ligands to NKG2D (expressed on NK cells), chemokines, and other SASP factors.
  • In vivo models of liver fibrosis have shown effective clearance of senescent cells by activated NK cells (Krizhanovsky et al., Cell 134(4):657-667, 2008).
  • Studies have described various models to study senescence including liver fibrosis (Krizhanovsky et al., Cell 134(4):657-667, 2008), osteoarthritis (Xu et al., J. Gerontol. A Biol. Sci. Med.
  • MERS-CoV Middle East Respiratory Syndrome
  • CD26 is the functional receptor for the entry of MERS-CoV in humans (Raj et al., J. Virol.88(3):1834-1838, 2014).
  • the engagement of the MERS-CoA spike protein S with CD26 mediates viral attachment and internalization.
  • the residues involved in the CD26 virus binding are identical to the ADA binding domain indicating a potential competition for CD26 binding (Lu et al., Nature 500(7461):227-231, 2013).
  • CD26 exerts its physiological roles either via its enzymatic activity by regulating many peptides or via its interactions with a variety of binding partners. Consequently, altered expression, and/or activity of CD26 have been implicated in several pathological processes, including inflammation, viral infection, immune-mediated diseases, tumor growth, cellular senescence, and metabolic diseases (Mentlein et al., Regul. Pept.85(1):9-24, 1999; Lambeir et al., Crit. Rev. Clin. Lab.
  • CD26 is a cell-surface targetable protein for drug development to treat a variety of diseases including viral infections and aging-related pathologies.
  • This application describes the identification of novel human-derived monoclonal antibodies and antigen-binding domains that specifically binding to human CD26.
  • proteins including an anti-CD26 antigen-binding domain where the anti-CD26 antigen-binding domain comprises: (a) a heavy chain variable domain comprising a CDR1 comprising SEQ ID NO: 1, a CDR2 comprising SEQ ID NO: 2, and a CDR3 comprising SEQ ID NO: 3, and a light chain variable domain comprising a CDR1 comprising SEQ ID NO: 4, a CDR2 comprising SEQ ID NO: 5, and a CDR3 comprising SEQ ID NO: 6; (b) a heavy chain variable domain comprising a CDR1 comprising SEQ ID NO: 7, a CDR2 comprising SEQ ID NO: 8, and a CDR3 comprising SEQ ID NO: 9, and a light chain
  • the antigen-binding domain comprises a heavy chain variable domain comprising a CDR1 comprising SEQ ID NO: 1, a CDR2 comprising SEQ ID NO: 2, and a CDR3 comprising SEQ ID NO: 3, and a light chain variable domain comprising a CDR1 comprising SEQ ID NO: 4, a CDR2 comprising SEQ ID NO: 5, and a CDR3 comprising SEQ ID NO: 6.
  • the heavy chain variable domain comprises a sequence that is at least 80% (e.g., at least 85%, at least 90%, at least 92%, at least 94%, at least 95%, at least 96%, at least 97%, at least 98%, at least 99%, or 100%) identical to SEQ ID NO: 61.
  • the light chain variable domain comprises a sequence that is at least 80% (e.g., at least 85%, at least 90%, at least 92%, at least 94%, at least 95%, at least 96%, at least 97%, at least 98%, at least 99%, or 100%) identical to SEQ ID NO: 62.
  • the antigen-binding domain comprises a heavy chain variable domain comprising a CDR1 comprising SEQ ID NO: 7, a CDR2 comprising SEQ ID NO: 8, and a CDR3 comprising SEQ ID NO: 9, and a light chain variable domain comprising a CDR1 comprising SEQ ID NO: 10, a CDR2 comprising SEQ ID NO: 11, and a CDR3 comprising SEQ ID NO: 12.
  • the heavy chain variable domain comprises a sequence that is at least 80% (e.g., at least 85%, at least 90%, at least 92%, at least 94%, at least 95%, at least 96%, at least 97%, at least 98%, at least 99%, or 100%) identical to SEQ ID NO: 63.
  • the light chain variable domain comprises a sequence that is at least 80% (e.g., at least 85%, at least 90%, at least 92%, at least 94%, at least 95%, at least 96%, at least 97%, at least 98%, at least 99%, or 100%) identical to SEQ ID NO: 64.
  • the antigen-binding domain comprises a heavy chain variable domain comprising a CDR1 comprising SEQ ID NO: 13, a CDR2 comprising SEQ ID NO: 14, and a CDR3 comprising SEQ ID NO: 15, and a light chain variable domain comprising a CDR1 comprising SEQ ID NO: 16, a CDR2 comprising SEQ ID NO: 17, and a CDR3 comprising SEQ ID NO: 18.
  • the heavy chain variable domain comprises a sequence that is at least 80% (e.g., at least 85%, at least 90%, at least 92%, at least 94%, at least 95%, at least 96%, at least 97%, at least 98%, at least 99%, or 100%) identical to SEQ ID NO: 65.
  • the light chain variable domain comprises a sequence that is at least 80% (e.g., at least 85%, at least 90%, at least 92%, at least 94%, at least 95%, at least 96%, at least 97%, at least 98%, at least 99%, or 100%) identical to SEQ ID NO: 66.
  • the antigen-binding domain comprises a heavy chain variable domain comprising a CDR1 comprising SEQ ID NO: 19, a CDR2 comprising SEQ ID NO: 20, and a CDR3 comprising SEQ ID NO: 21, and a light chain variable domain comprising a CDR1 comprising SEQ ID NO: 22, a CDR2 comprising SEQ ID NO: 23, and a CDR3 comprising SEQ ID NO: 24.
  • the heavy chain variable domain comprises a sequence that is at least 80% (e.g., at least 85%, at least 90%, at least 92%, at least 94%, at least 95%, at least 96%, at least 97%, at least 98%, at least 99%, or 100%) identical to SEQ ID NO: 67.
  • the light chain variable domain comprises a sequence that is at least 80% (e.g., at least 85%, at least 90%, at least 92%, at least 94%, at least 95%, at least 96%, at least 97%, at least 98%, at least 99%, or 100%) identical to SEQ ID NO: 68.
  • the antigen-binding domain comprises a heavy chain variable domain comprising a CDR1 comprising SEQ ID NO: 25, a CDR2 comprising SEQ ID NO: 26, and a CDR3 comprising SEQ ID NO: 27, and a light chain variable domain comprising a CDR1 comprising SEQ ID NO: 28, a CDR2 comprising SEQ ID NO: 29, and a CDR3 comprising SEQ ID NO: 30.
  • the heavy chain variable domain comprises a sequence that is at least 80% (e.g., at least 85%, at least 90%, at least 92%, at least 94%, at least 95%, at least 96%, at least 97%, at least 98%, at least 99%, or 100%) identical to SEQ ID NO: 69.
  • the light chain variable domain comprises a sequence that is at least 80% (e.g., at least 85%, at least 90%, at least 92%, at least 94%, at least 95%, at least 96%, at least 97%, at least 98%, at least 99%, or 100%) identical to SEQ ID NO: 70.
  • the antigen-binding domain comprises a heavy chain variable domain comprising a CDR1 comprising SEQ ID NO: 31, a CDR2 comprising SEQ ID NO: 32, and a CDR3 comprising SEQ ID NO: 33, and a light chain variable domain comprising a CDR1 comprising SEQ ID NO: 34, a CDR2 comprising SEQ ID NO: 35, and a CDR3 comprising SEQ ID NO: 36.
  • the heavy chain variable domain comprises a sequence that is at least 80% (e.g., at least 85%, at least 90%, at least 92%, at least 94%, at least 95%, at least 96%, at least 97%, at least 98%, at least 99%, or 100%) identical to SEQ ID NO: 71.
  • the light chain variable domain comprises a sequence that is at least 80% (e.g., at least 85%, at least 90%, at least 92%, at least 94%, at least 95%, at least 96%, at least 97%, at least 98%, at least 99%, or 100%) identical to SEQ ID NO: 72.
  • the antigen-binding domain comprises a heavy chain variable domain comprising a CDR1 comprising SEQ ID NO: 37, a CDR2 comprising SEQ ID NO: 38, and a CDR3 comprising SEQ ID NO: 39, and a light chain variable domain comprising a CDR1 comprising SEQ ID NO: 40, a CDR2 comprising SEQ ID NO: 41, and a CDR3 comprising SEQ ID NO: 42.
  • the heavy chain variable domain comprises a sequence that is at least 80% (e.g., at least 85%, at least 90%, at least 92%, at least 94%, at least 95%, at least 96%, at least 97%, at least 98%, at least 99%, or 100%) identical to SEQ ID NO: 73.
  • the light chain variable domain comprises a sequence that is at least 80% (e.g., at least 85%, at least 90%, at least 92%, at least 94%, at least 95%, at least 96%, at least 97%, at least 98%, at least 99%, or 100%) identical to SEQ ID NO: 74.
  • the antigen-binding domain comprises a heavy chain variable domain comprising a CDR1 comprising SEQ ID NO: 43, a CDR2 comprising SEQ ID NO: 44, and a CDR3 comprising SEQ ID NO: 45, and a light chain variable domain comprising a CDR1 comprising SEQ ID NO: 46, a CDR2 comprising SEQ ID NO: 47, and a CDR3 comprising SEQ ID NO: 48.
  • the heavy chain variable domain comprises a sequence that is at least 80% (e.g., at least 85%, at least 90%, at least 92%, at least 94%, at least 95%, at least 96%, at least 97%, at least 98%, at least 99%, or 100%) identical to SEQ ID NO: 75.
  • the light chain variable domain comprises a sequence that is at least 80% (e.g., at least 85%, at least 90%, at least 92%, at least 94%, at least 95%, at least 96%, at least 97%, at least 98%, at least 99%, or 100%) identical to SEQ ID NO: 76.
  • the antigen-binding domain comprises a heavy chain variable domain comprising a CDR1 comprising SEQ ID NO: 49, a CDR2 comprising SEQ ID NO: 50, and a CDR3 comprising SEQ ID NO: 51, and a light chain variable domain comprising a CDR1 comprising SEQ ID NO: 52, a CDR2 comprising SEQ ID NO: 53, and a CDR3 comprising SEQ ID NO: 54.
  • the heavy chain variable domain comprises a sequence that is at least 80% (e.g., at least 85%, at least 90%, at least 92%, at least 94%, at least 95%, at least 96%, at least 97%, at least 98%, at least 99%, or 100%) identical to SEQ ID NO: 77.
  • the light chain variable domain comprises a sequence that is at least 80% (e.g., at least 85%, at least 90%, at least 92%, at least 94%, at least 95%, at least 96%, at least 97%, at least 98%, at least 99%, or 100%) identical to SEQ ID NO: 78.
  • the antigen-binding domain comprises a heavy chain variable domain comprising a CDR1 comprising SEQ ID NO: 55, a CDR2 comprising SEQ ID NO: 56, and a CDR3 comprising SEQ ID NO: 57, and a light chain variable domain comprising a CDR1 comprising SEQ ID NO: 58, a CDR2 comprising SEQ ID NO: 59, and a CDR3 comprising SEQ ID NO: 60.
  • the heavy chain variable domain comprises a sequence that is at least 80% (e.g., at least 85%, at least 90%, at least 92%, at least 94%, at least 95%, at least 96%, at least 97%, at least 98%, at least 99%, or 100%) identical to SEQ ID NO: 79.
  • the light chain variable domain comprises a sequence that is at least 80% (e.g., at least 85%, at least 90%, at least 92%, at least 94%, at least 95%, at least 96%, at least 97%, at least 98%, at least 99%, or 100%) identical to SEQ ID NO: 80.
  • CD26 Ab-01D Heavy Chain Variable Domain CDR1 (SEQ ID NO: 1) TINDSYIH CD26 Ab-01D Heavy Chain Variable Domain CDR2 (SEQ ID NO: 2) WIWPYGGFTY CD26 Ab-01D Heavy Chain Variable Domain CDR3 (SEQ ID NO: 3) ARFLGSSSIMDY CD26 Ab-01D Light Chain Variable Domain CDR1 (SEQ ID NO: 4) RASQDVNSNVA CD26 Ab-01D Light Chain Variable Domain CDR2 (SEQ ID NO: 5) FGSGGLYS CD26 Ab-01D Light Chain Variable Domain CDR3 (SEQ ID NO: 6) QQYSSYPL CD26 Ab-04A Heavy Chain Variable Domain CDR1 (SEQ ID NO: 7) AINNYSIH CD26 Ab-04A Heavy Chain Variable Domain CDR2 (SEQ ID NO: 8) SIWPYGGFTS CD26 Ab-04A Heavy Chain Variable Domain CDR3 (SEQ ID NO: 9) ARFFSSYGDMDY CD26 Ab-04A Light Chain Variable Domain
  • any of the proteins described herein can include an antigen-binding domain that includes a heavy chain variable domain that comprises a sequence that is at least 80% identical (e.g., at least 85% identical, at least 90% identical, at least 92% identical, at least 94% identical, at least 96% identical, at least 98% identical, at least 99% identical, or 100% identical) to SEQ ID NO: 63, and a light chain variable domain that comprises a sequence that is at least 80% identical (e.g., at least 85% identical, at least 90% identical, at least 92% identical, at least 94% identical, at least 96% identical, at least 98% identical, at least 99% identical, or 100% identical) to SEQ ID NO: 64.
  • any of the proteins described herein can include an antigen-binding domain that includes a heavy chain variable domain that comprises a sequence that is at least 80% identical (e.g., at least 85% identical, at least 90% identical, at least 92% identical, at least 94% identical, at least 96% identical, at least 98% identical, at least 99% identical, or 100% identical) to SEQ ID NO: 65, and a light chain variable domain that comprises a sequence that is at least 80% identical (e.g., at least 85% identical, at least 90% identical, at least 92% identical, at least 94% identical, at least 96% identical, at least 98% identical, at least 99% identical, or 100% identical) to SEQ ID NO: 66.
  • any of the proteins described herein can include an antigen-binding domain that includes a heavy chain variable domain that comprises a sequence that is at least 80% identical (e.g., at least 85% identical, at least 90% identical, at least 92% identical, at least 94% identical, at least 96% identical, at least 98% identical, at least 99% identical, or 100% identical) to SEQ ID NO: 67, and a light chain variable domain that comprises a sequence that is at least 80% identical (e.g., at least 85% identical, at least 90% identical, at least 92% identical, at least 94% identical, at least 96% identical, at least 98% identical, at least 99% identical, or 100% identical) to SEQ ID NO: 68).
  • an antigen-binding domain that includes a heavy chain variable domain that comprises a sequence that is at least 80% identical (e.g., at least 85% identical, at least 90% identical, at least 92% identical, at least 94% identical, at least 96% identical, at least 98% identical, at least 99% identical, or 100% identical
  • any of the proteins described herein can include an antigen-binding domain that includes a heavy chain variable domain that comprises a sequence that is at least 80% identical (e.g., at least 85% identical, at least 90% identical, at least 92% identical, at least 94% identical, at least 96% identical, at least 98% identical, at least 99% identical, or 100% identical) to SEQ ID NO: 69, and a light chain variable domain that comprises a sequence that is at least 80% identical (e.g., at least 85% identical, at least 90% identical, at least 92% identical, at least 94% identical, at least 96% identical, at least 98% identical, at least 99% identical, or 100% identical) to SEQ ID NO: 70.
  • an antigen-binding domain that includes a heavy chain variable domain that comprises a sequence that is at least 80% identical (e.g., at least 85% identical, at least 90% identical, at least 92% identical, at least 94% identical, at least 96% identical, at least 98% identical, at least 99% identical, or 100% identical)
  • any of the proteins described herein can include an antigen-binding domain that includes a heavy chain variable domain that comprises a sequence that is at least 80% identical (e.g., at least 85% identical, at least 90% identical, at least 92% identical, at least 94% identical, at least 96% identical, at least 98% identical, at least 99% identical, or 100% identical) to SEQ ID NO: 71, and a light chain variable domain that comprises a sequence that is at least 80% identical (e.g., at least 85% identical, at least 90% identical, at least 92% identical, at least 94% identical, at least 96% identical, at least 98% identical, at least 99% identical, or 100% identical) to SEQ ID NO: 72.
  • an antigen-binding domain that includes a heavy chain variable domain that comprises a sequence that is at least 80% identical (e.g., at least 85% identical, at least 90% identical, at least 92% identical, at least 94% identical, at least 96% identical, at least 98% identical, at least 99% identical, or 100% identical)
  • any of the proteins described herein can include an antigen-binding domain that includes a heavy chain variable domain that comprises a sequence that is at least 80% identical (e.g., at least 85% identical, at least 90% identical, at least 92% identical, at least 94% identical, at least 96% identical, at least 98% identical, at least 99% identical, or 100% identical) to SEQ ID NO: 73, and a light chain variable domain that comprises a sequence that is at least 80% identical (e.g., at least 85% identical, at least 90% identical, at least 92% identical, at least 94% identical, at least 96% identical, at least 98% identical, at least 99% identical, or 100% identical) to SEQ ID NO: 74.
  • an antigen-binding domain that includes a heavy chain variable domain that comprises a sequence that is at least 80% identical (e.g., at least 85% identical, at least 90% identical, at least 92% identical, at least 94% identical, at least 96% identical, at least 98% identical, at least 99% identical, or 100% identical
  • any of the proteins described herein can include an antigen-binding domain that includes a heavy chain variable domain that comprises a sequence that is at least 80% identical (e.g., at least 85% identical, at least 90% identical, at least 92% identical, at least 94% identical, at least 96% identical, at least 98% identical, at least 99% identical, or 100% identical) to SEQ ID NO: 75, and a light chain variable domain that comprises a sequence that is at least 80% identical (e.g., at least 85% identical, at least 90% identical, at least 92% identical, at least 94% identical, at least 96% identical, at least 98% identical, at least 99% identical, or 100% identical) to SEQ ID NO: 76).
  • any of the proteins described herein can include an antigen-binding domain that includes a heavy chain variable domain that comprises a sequence that is at least 80% identical (e.g., at least 85% identical, at least 90% identical, at least 92% identical, at least 94% identical, at least 96% identical, at least 98% identical, at least 99% identical, or 100% identical) to SEQ ID NO: 77, and a light chain variable domain that comprises a sequence that is at least 80% identical (e.g., at least 85% identical, at least 90% identical, at least 92% identical, at least 94% identical, at least 96% identical, at least 98% identical, at least 99% identical, or 100% identical) to SEQ ID NO: 78.
  • an antigen-binding domain that includes a heavy chain variable domain that comprises a sequence that is at least 80% identical (e.g., at least 85% identical, at least 90% identical, at least 92% identical, at least 94% identical, at least 96% identical, at least 98% identical, at least 99% identical, or 100% identical
  • any of the proteins described herein can include an antigen-binding domain that includes a heavy chain variable domain that comprises a sequence that is at least 80% identical (e.g., at least 85% identical, at least 90% identical, at least 92% identical, at least 94% identical, at least 96% identical, at least 98% identical, at least 99% identical, or 100% identical) to SEQ ID NO: 79, and a light chain variable domain that comprises a sequence that is at least 80% identical (e.g., at least 85% identical, at least 90% identical, at least 92% identical, at least 94% identical, at least 96% identical, at least 98% identical, at least 99% identical, or 100% identical) to SEQ ID NO: 80.
  • any of the proteins described herein can include an antigen-binding domain that includes a heavy chain variable domain encoded by a nucleic acid that comprises a sequence that is at least 80% identical (e.g., at least 85% identical, at least 90% identical, at least 92% identical, at least 94% identical, at least 96% identical, at least 98% identical, at least 99% identical, or 100% identical) to SEQ ID NO: 81, and a light chain variable domain encoded by a nucleic acid that comprises a sequence that is at least 80% identical (e.g., at least 85% identical, at least 90% identical, at least 92% identical, at least 94% identical, at least 96% identical, at least 98% identical, at least 99% identical, or 100% identical) to SEQ ID NO: 82.
  • any of the proteins described herein can include an antigen-binding domain that includes a heavy chain variable domain encoded by a nucleic acid that comprises a sequence that is at least 80% identical (e.g., at least 85% identical, at least 90% identical, at least 92% identical, at least 94% identical, at least 96% identical, at least 98% identical, at least 99% identical, or 100% identical) to SEQ ID NO: 83, and a light chain variable domain encoded by a nucleic acid that comprises a sequence that is at least 80% identical (e.g., at least 85% identical, at least 90% identical, at least 92% identical, at least 94% identical, at least 96% identical, at least 98% identical, at least 99% identical, or 100% identical) to SEQ ID NO: 84.
  • any of the proteins described herein can include an antigen-binding domain that includes a heavy chain variable domain encoded by a nucleic acid that comprises a sequence that is at least 80% identical (e.g., at least 85% identical, at least 90% identical, at least 92% identical, at least 94% identical, at least 96% identical, at least 98% identical, at least 99% identical, or 100% identical) to SEQ ID NO: 85, and a light chain variable domain encoded by a nucleic acid that comprises a sequence that is at least 80% identical (e.g., at least 85% identical, at least 90% identical, at least 92% identical, at least 94% identical, at least 96% identical, at least 98% identical, at least 99% identical, or 100% identical) to SEQ ID NO: 86.
  • any of the proteins described herein can include an antigen-binding domain that includes a heavy chain variable domain encoded by a nucleic acid that comprises a sequence that is at least 80% identical (e.g., at least 85% identical, at least 90% identical, at least 92% identical, at least 94% identical, at least 96% identical, at least 98% identical, at least 99% identical, or 100% identical) to SEQ ID NO: 87, and a light chain variable domain encoded by a nucleic acid that comprises a sequence that is at least 80% identical (e.g., at least 85% identical, at least 90% identical, at least 92% identical, at least 94% identical, at least 96% identical, at least 98% identical, at least 99% identical, or 100% identical) to SEQ ID NO: 88.
  • any of the proteins described herein can include an antigen-binding domain that includes a heavy chain variable domain encoded by a nucleic acid that comprises a sequence that is at least 80% identical (e.g., at least 85% identical, at least 90% identical, at least 92% identical, at least 94% identical, at least 96% identical, at least 98% identical, at least 99% identical, or 100% identical) to SEQ ID NO: 89, and a light chain variable domain encoded by a nucleic acid that comprises a sequence that is at least 80% identical (e.g., at least 85% identical, at least 90% identical, at least 92% identical, at least 94% identical, at least 96% identical, at least 98% identical, at least 99% identical, or 100% identical) to SEQ ID NO: 90.
  • any of the proteins described herein can include an antigen-binding domain that includes a heavy chain variable domain encoded by a nucleic acid that comprises a sequence that is at least 80% identical (e.g., at least 85% identical, at least 90% identical, at least 92% identical, at least 94% identical, at least 96% identical, at least 98% identical, at least 99% identical, or 100% identical) to SEQ ID NO: 91, and a light chain variable domain encoded by a nucleic acid that comprises a sequence that is at least 80% identical (e.g., at least 85% identical, at least 90% identical, at least 92% identical, at least 94% identical, at least 96% identical, at least 98% identical, at least 99% identical, or 100% identical) to SEQ ID NO: 92.
  • any of the proteins described herein can include an antigen-binding domain that includes a heavy chain variable domain encoded by a nucleic acid that comprises a sequence that is at least 80% identical (e.g., at least 85% identical, at least 90% identical, at least 92% identical, at least 94% identical, at least 96% identical, at least 98% identical, at least 99% identical, or 100% identical) to SEQ ID NO: 93, and a light chain variable domain encoded by a nucleic acid that comprises a sequence that is at least 80% identical (e.g., at least 85% identical, at least 90% identical, at least 92% identical, at least 94% identical, at least 96% identical, at least 98% identical, at least 99% identical, or 100% identical) to SEQ ID NO: 94.
  • any of the proteins described herein can include an antigen-binding domain that includes a heavy chain variable domain encoded by a nucleic acid that comprises a sequence that is at least 80% identical (e.g., at least 85% identical, at least 90% identical, at least 92% identical, at least 94% identical, at least 96% identical, at least 98% identical, at least 99% identical, or 100% identical) to SEQ ID NO: 95, and a light chain variable domain encoded by a nucleic acid that comprises a sequence that is at least 80% identical (e.g., at least 85% identical, at least 90% identical, at least 92% identical, at least 94% identical, at least 96% identical, at least 98% identical, at least 99% identical, or 100% identical) to SEQ ID NO: 96.
  • any of the proteins described herein can include an antigen-binding domain that includes a heavy chain variable domain encoded by a nucleic acid that comprises a sequence that is at least 80% identical (e.g., at least 85% identical, at least 90% identical, at least 92% identical, at least 94% identical, at least 96% identical, at least 98% identical, at least 99% identical, or 100% identical) to SEQ ID NO: 97, and a light chain variable domain encoded by a nucleic acid that comprises a sequence that is at least 80% identical (e.g., at least 85% identical, at least 90% identical, at least 92% identical, at least 94% identical, at least 96% identical, at least 98% identical, at least 99% identical, or 100% identical) to SEQ ID NO: 98.
  • any of the proteins described herein can include an antigen-binding domain that includes a heavy chain variable domain encoded by a nucleic acid that comprises a sequence that is at least 80% identical (e.g., at least 85% identical, at least 90% identical, at least 92% identical, at least 94% identical, at least 96% identical, at least 98% identical, at least 99% identical, or 100% identical) to SEQ ID NO: 99, and a light chain variable domain encoded by a nucleic acid that comprises a sequence that is at least 80% identical (e.g., at least 85% identical, at least 90% identical, at least 92% identical, at least 94% identical, at least 96% identical, at least 98% identical, at least 99% identical, or 100% identical) to SEQ ID NO: 100.
  • the proteins can be single-chain polypeptides. In some embodiments, the proteins can be multi-chain polypeptides. In some examples, the proteins described herein can be an antibody, antigen-binding antibody fragment, or a chimeric antigen receptor.
  • Antigen-Binding Domains The antigen-binding domains present in any of the proteins described herein (e.g., single- or multi-chain proteins) described herein are each independently selected from the group consisting of: a VHH domain, a VNAR domain, and a scFv.
  • any of the antigen-binding domains described herein is a BiTe, a (scFv)2, a nanobody, a nanobody-HSA, a DART, a TandAb, a scDiabody, a scDiabody-CH3, scFv- CH-CL-scFv, a HSAbody, scDiabody-HAS, or a tandem-scFv.
  • Additional examples of antigen-binding domains that can be used in any of the proteins described herein are known in the art.
  • a VHH domain is a single monomeric variable antibody domain that can be found in camelids.
  • a VNAR domain is a single monomeric variable antibody domain that can be found in cartilaginous fish.
  • VHH domains and VNAR domains are described in, e.g., Cromie et al., Curr. Top. Med. Chem.15:2543- 2557, 2016; De Genst et al., Dev. Comp. Immunol.30:187-198, 2006; De Meyer et al., Trends Biotechnol.32:263-270, 2014; Kijanka et al., Nanomedicine 10:161-174, 2015; Kovaleva et al., Expert. Opin. Biol. Ther.14:1527-1539, 2014; Krah et al., Immunopharmacol.
  • two or more of polypeptides present in the multi-chain protein can assemble (e.g., non-covalently assemble) to form any of the antigen-binding domains described herein, e.g., an antigen-binding fragment of an antibody (e.g., any of the antigen-binding fragments of an antibody described herein), a VHH-scAb, a VHH- Fab, a Dual scFab, a F(ab’)2, a diabody, a crossMab, a DAF (two-in-one), a DAF (four- in-one), a DutaMab, a DT-IgG, a knobs-in-holes common light chain, a
  • Non- limiting examples of an antigen-binding fragment of an antibody include an Fv fragment, a Fab fragment, a F(ab') 2 fragment, and a Fab' fragment.
  • an antigen-binding fragment of an antibody is an antigen-binding fragment of an IgG (e.g., an antigen-binding fragment of IgG1, IgG2, IgG3, or IgG4) (e.g., an antigen-binding fragment of a human or humanized IgG, e.g., human or humanized IgG1, IgG2, IgG3, or IgG4); an antigen-binding fragment of an IgA (e.g., an antigen-binding fragment of IgA1 or IgA2) (e.g., an antigen-binding fragment of a human or humanized IgA, e.g., a human or humanized IgA1 or IgA2); an antigen-binding fragment of an IgD (e.g., an antigen- binding fragment of a human or humanized IgD); an antigen-binding fragment of an IgE (e.g., an antigen-binding fragment of a human or
  • An “Fv” fragment includes a non-covalently-linked dimer of one heavy chain variable domain and one light chain variable domain.
  • a “Fab” fragment includes, the constant domain of the light chain and the first constant domain (CH1) of the heavy chain, in addition to the heavy and light chain variable domains of the Fv fragment.
  • a “F(ab')2” fragment includes two Fab fragments joined, near the hinge region, by disulfide bonds.
  • a “dual variable domain immunoglobulin” or “DVD-Ig” refers to multivalent and multispecific binding proteins as described, e.g., in DiGiammarino et al., Methods Mol.
  • a protein described herein can be an antibody (e.g., a human or humanized antibody).
  • an antibody can be a human or humanized IgG, e.g., a human or humanized IgG1, IgG2, IgG3, or IgG4.
  • an antibody can be a human or humanized IgA (e.g., a human or humanized IgA1 or IgA2).
  • an antibody can be a human or humanized IgD, a human or humanized IgE, or a human or humanized IgM.
  • any of the proteins described herein can include an Fc receptor (e.g., an Fc receptor including three substitutions of S239D, A330L, and I332E).
  • Chimeric Antigen Receptors in some embodiments, can be a chimeric antigen receptor.
  • Chimeric antigen receptors include an extracellular antigen-binding domain (e.g., any of the anti-CD26 antigen-binding domains described herein), a transmembrane domain, a costimulatory domain (e.g., an intracellular CD28 domain), and a CD3zeta signaling domain.
  • a chimeric antigen receptor can include an extracellular antigen-binding domain (e.g., any of the anti-CD26 antigen-binding domains described herein), a transmembrane domain (e.g., a CD8 alpha transmembrane domain), a CD28 intracellular signaling domain, and a CD3zeta intracellular signaling domain.
  • a chimeric antigen receptor can include a hinge region (e.g., a CD8 alpha hinge region) disposed between the extracellular antigen-binding domain and the transmembrane domain.
  • a hinge region can comprise a sequence that is at least 80% identical (e.g., at least 85%, at least 90%, at least 92%, at least 94%, at least 96%, at least 98%, at least 99%, or 100% identical) to SEQ ID NO: 254.
  • a hinge region can be encoded by a sequence that is at least 80% identical (e.g., at least 85%, at least 90%, at least 92%, at least 94%, at least 96%, at least 98%, at least 99%, or 100% identical) to SEQ ID NO: 255.
  • a transmembrane domain can include a sequence that is at least 80%, at least 85%, at least 90%, at least 95%, at least 99%, or 100% identical to SEQ ID NO: 101 (FWVLVVVGGVLACYSLLVTVAFIIFWV).
  • a transmembrane domain can be a transmembrane domain from CD28 (e.g., human CD28).
  • a chimeric antigen receptor can include a transmembrane and cytoplasmic signaling domain from CD28 that includes a sequence that is at least 80% identical (e.g., at least 85%, at least 90%, at least 92%, at least 94%, at least 96%, at least 98%, at least 99%, or 100% identical) to SEQ ID NO: 256.
  • the transmembrane and cytoplasmic signaling domain from CD28 can be encoded by a sequence that is at least 80% identical (e.g., at least 85%, at least 90%, at least 92%, at least 94%, at least 96%, at least 98%, at least 99%, or 100% identical) to SEQ ID NO: 257.
  • a costimulatory domain can include a sequence that is at least 80%, at least 85%, at least 90%, at least 95%, at least 99%, or 100% identical to SEQ ID NO: 102 (RSKRSRLLHSDYMNMTPRRPGPTRKHYQPYAPPRDFAAYRS).
  • a CD3zeta signaling domain can include a sequence that is at least 80%, at least 85%, at least 90%, at least 95%, at least 99%, or 100% identical to SEQ ID NO: 103
  • a CD3zeta signaling domain can include a sequence that is at least 80% (e.g., at least 85%, at least 90%, at least 92%, at least 94%, at least 96%, at least 98%, at least 99%, or 100% identical) to SEQ ID NO: 258.
  • a CD3zeta signaling domain is encoded by a sequence that is at least 80% identical (e.g., at least 85%, at least 90%, at least 92%, at least 94%, at least 96%, at least 98%, at least 99%, or 100% identical) to SEQ ID NO: 259.
  • Human CD3zeta Signaling Domain (SEQ ID NO: 258)
  • Human CD3zeta Signaling Domain (SEQ ID NO: 259)
  • a chimeric antigen receptor can include a sequence that is at least 80% identical (e.g., at least 85%, at least 90%, at least 92%, at least 94%, at least 96%, at least 98%, at least 99%, or 100% identical) to SEQ ID NO: 253.
  • a chimeric antigen receptor can be encoded by a sequence that is at least 80% identical (e.g., at least 85%, at least 90%, at least 92%, at least 94%, at least 96%, at least 98%, at least 99% or 100% identical) to SEQ ID NO: 252.
  • Exemplary Anti-CD26 Chimeric Antigen Receptor (with Signal Sequence) SEQ ID NO: 253
  • Exemplary Anti-CD26 Chimeric Antigen Receptor with Signal Sequence
  • a chimeric antigen receptor can include a sequence that is at least 80% identical (e.g., at least 85%, at least 90%, at least 92%, at least 94%, at least 96%, at least 98%, at least 99%, or 100% identical) to SEQ ID NO: 260.
  • a chimeric antigen receptor can be encoded by a sequence that is at least 80% identical (e.g., at least 85%, at least 90%, at least 92%, at least 94%, at least 96%, at least 98%, at least 99% or 100% identical) to SEQ ID NO: 261.
  • nucleic acids that include a sequence that encodes any of the proteins described herein.
  • a set of nucleic acids that together include sequences that encode any of the multi-chain proteins described herein.
  • vectors that include a sequence that encode any of the proteins described herein.
  • sets of vectors that together include sequences that encode any of the multi-chain proteins described herein. Non-limiting examples of vectors include expression vectors.
  • expression vectors include viral vectors (e.g., a lentivirus vector, an adeno-associated virus vector, or a retrovirus vector). Some embodiments of any of the vectors or nucleic acids described herein can further include a promoter operably linked to a sequence or sequences encoding the protein.
  • Cells Also provided herein are cells including a nucleic acid encoding any of the proteins described herein, or a vector comprising any of the nucleic acids described herein. In some examples of any of the cells described herein, the cell is an immune cell.
  • the cell is a production cell line, including by not limited to Chinese Hamster ovary (CHO) cells (e.g., CHO.K1, CD-CHO, CHO-S, GS CHO, CHO-DG44, etc.), HEK293, Cos, NS0, Sp2/0, and PerC6 cells.
  • CHO Chinese Hamster ovary
  • an “immune cell” refers to a cell of the immune system which can be categorized as lymphocytes (e.g., T cells, B cells, and NK cells), neutrophils, and monocytes/macrophages.
  • the immune cell is a T cell, a B cell, or a natural killer (NK) cell.
  • the immune cell can be a T cell, e.g., a CD4+ T cell, a CD8+ T cell, a Treg cell, a Th1 T cell, a Th2 T cell, a Th17 T cell, an unspecific T cell, or a population of T cells that comprises a combination thereof.
  • compositions e.g., pharmaceutical compositions
  • compositions that include at least one of any of the proteins described herein or any of the cells described herein.
  • compositions e.g., pharmaceutical compositions
  • compositions that include at least one of any of the nucleic acids described herein or any of the vectors described herein.
  • the compositions can be disposed in a sterile vial or a pre-loaded syringe.
  • the compositions e.g., pharmaceutical compositions
  • are formulated for different routes of administration e.g., intravenous, subcutaneous, intramuscular, or intratumoral.
  • the compositions e.g., pharmaceutical compositions
  • can include a pharmaceutically acceptable carrier e.g., phosphate buffered saline.
  • Single or multiple administrations of any of the pharmaceutical compositions described herein can be given to a subject depending on, for example: the dosage and frequency as required and tolerated by the patient.
  • a dosage of the pharmaceutical composition should provide a sufficient quantity of the protein, nucleic acid, vector, or cell to effectively treat or ameliorate conditions, diseases, or symptoms.
  • methods of treating a subject having a cancer e.g., any of the cancers described herein
  • methods of treating a subject having a cancer that include administering a therapeutically effective amount of at least one of any of the compositions or pharmaceutical compositions provided herein.
  • Kits Also provided herein are kits that include any of the pharmaceutical compositions described herein. In some embodiments, the kits can include instructions for performing any of the methods described herein. In some embodiments, the kits can include at least one dose of any of the compositions (e.g., pharmaceutical compositions) described herein.
  • kits can provide a syringe for administering any of the pharmaceutical compositions described herein.
  • Methods of Treating Age-Related and Inflammatory Disease in a Subject Provided herein are methods of treating an age-related disease or an inflammatory disease in a subject, that include administering a therapeutically effective amount of any of the proteins described herein or any of the pharmaceutical compositions described herein. Also provided herein are methods of treating an age-related disease or an inflammatory disease in a subject, that include administering a therapeutically effective amount of any of the nucleic acids described herein or any of the pharmaceutical compositions described herein.
  • the methods further include administering: (i) a therapeutically effective amount of an NK cell activating agent and/or an NK cell and/or monoclonal antibody; and (ii) a therapeutically effective amount of a Treg cell activating agent and/or a Treg cell and/or a monoclonal antibody and/or an advanced glycation end product (AGE) inhibitor.
  • the age-related disease is inflamm-aging related.
  • Also provided herein are methods of treating an age-related disease or an inflammatory disease that include administering: (i) a therapeutically effective amount of an NK cell activating agent and/or an NK cell and/or monoclonal antibody; and (ii) a therapeutically effective amount of a Treg cell activating agent and/or a Treg cell and/or a monoclonal antibody and/or an advanced glycation end product (AGE) inhibitor.
  • a therapeutically effective amount of an NK cell activating agent and/or an NK cell and/or monoclonal antibody a therapeutically effective amount of a Treg cell activating agent and/or a Treg cell and/or a monoclonal antibody and/or an advanced glycation end product (AGE) inhibitor.
  • AGE advanced glycation end product
  • (ii) is administered to the subject prior to administration of (i) to the subject.
  • the subject is administered the protein, the cell, or the nucleic acid at substantially the same time as (i) and (ii).
  • the subject is administered the protein, the cell, or the nucleic acid prior to the administration of (i) and (ii).
  • the subject is administered the protein, the cell, or the nucleic acid after the administration of (i) and (ii).
  • the method includes administering a therapeutically effective amount of an NK cell to the subject.
  • the NK cell is an autologous NK cell.
  • the method can further include: isolating the NK cell from the subject; and culturing the isolated NK cell in a liquid culture medium under conditions sufficient to induce or increase proliferation of the NK cell, where following the isolating and culturing steps, the NK cell is administered to the subject.
  • the liquid culture medium includes one or more multi-chain chimeric polypeptide(s) (e.g., any of the exemplary multi-chain chimeric polypeptide(s) described herein).
  • the NK cell includes a chimeric antigen receptor (e.g., a chimeric antigen receptor comprises an extracellular domain that binds specifically to tissue factor or CD26) (e.g., any of the chimeric antigen receptors described herein that include any of the anti-CD26 antigen-binding domains described herein).
  • the method can include administering a therapeutically effective amount of an NK cell activating agent to the subject.
  • the NK cell activating agent is one or more multi-chain chimeric polypeptide(s) (e.g., one or more of any of the multi-chain chimeric polypeptides described herein).
  • the NK cell activating agent is one or more of an anti-tissue factor antibody, an anti-CD26 antibody (e.g., any of the anti-CD26 antibodies described herein), and/or an anti-CD36 antibody.
  • the NK cell activating agent includes one or more multi-chain chimeric polypeptide(s) and one or more of an anti- tissue factor antibody, an anti-CD26 antibody (e.g., any of the anti-CD26 antibodies described herein), and/or an anti-CD36 antibody.
  • the method includes administering a therapeutically effective amount of a Treg cell to the subject.
  • the Treg cell is an autologous Treg cell.
  • the method further includes: isolating the Treg cell from the subject; culturing the isolated Treg cell in a liquid culture medium under conditions sufficient to induce or increase proliferation of the Treg cell, where following the isolating and culturing steps, the Treg cell is administered to the subject.
  • the liquid culture medium includes one or more single-chain chimeric polypeptide(s).
  • the Treg cell includes a chimeric antigen receptor (e.g., a chimeric antigen receptor including an extracellular domain that binds specifically to tissue factor, CD26 (e.g., any of the anti-CD26 antibodies described herein), and/or CD36).
  • the method includes administering a therapeutically effective amount of a Treg cell activating agent to the subject.
  • the Treg cell activating agent is one or more single-chain chimeric polypeptide(s) (e.g., one or more of any of the single-chain chimeric polypeptides described herein).
  • the Treg cell activating agent is one or both of an anti-tissue factor antibody, anti-CD26 antibody (e.g., any of the anti-CD26 antibodies described herein), and/or an anti-CD36 antibody.
  • the Treg cell activating agent is a soluble RAGE trap.
  • the Treg cell activating agent includes one or more single- chain chimeric polypeptide(s) and one or more of an anti-tissue factor antibody, an anti- CD26 antibody (e.g., any of the anti-CD26 antibodies described herein), an anti-CD36 antibody, and a soluble RAGE trap.
  • the method includes administering a therapeutically effective amount of a monoclonal antibody to the subject.
  • a monoclonal antibody comprises one or more of an anti-tissue factor antibody, anti-CD26 antibody (e.g., any of the anti-CD26 antibodies described herein), and/or anti-CD36 antibody that can directly or indirectly reduce inflammasome or senescent cell activity.
  • the method includes administering a therapeutically effective amount of an advanced glycation end product (AGE) inhibitor to the subject.
  • an advanced glycation end product (AGE) inhibitor comprises one or more of soluble RAGE trap that can directly or indirectly reduce inflammasome or senescent cell activity.
  • the aging-related disease is inflamm-aging related.
  • Non-limiting examples of aging-related disease is selected from the group consisting of: Alzheimer’s disease, aneurysm, cystic fibrosis, fibrosis in pancreatitis, glaucoma, hypertension, idiopathic pulmonary fibrosis, inflammatory bowel disease, intervertebral disc degeneration, macular degeneration, osteoarthritis, type 2 diabetes mellitus, adipose atrophy, lipodystrophy, atherosclerosis, cataracts, COPD, idiopathic pulmonary fibrosis, kidney transplant failure, liver fibrosis, loss of bone mass, myocardial infarction, sarcopenia, wound healing, alopecia, cardiomyocyte hypertrophy, osteoarthritis, Parkinson’s disease, age-associated loss of lung tissue elasticity, macular degeneration, cachexia, glomerulosclerosis, liver cirrhosis, NAFLD, osteoporosis, amyotrophic lateral sclerosis, Huntington’s disease,
  • Non -limiting examples of inflammatory diseases include: rheumatoid arthritis, inflammatory bowel disease, lupus erythematosus, lupus nephritis, amyotrophic lateral sclerosis, diabetic nephropathy, CNS injury, Alzheimer’s disease, Parkinson’s disease, Crohn’s disease, multiple sclerosis, Guillain-Barre syndrome, psoriasis, Grave’s disease, ulcerative colitis, nonalcoholic steatohepatitis, and mood disorders.
  • the age-related disease is a cancer.
  • Non-limiting examples of cancer are selected from the group consisting of: solid tumor, hematological tumor, sarcoma, osteosarcoma, glioblastoma, neuroblastoma, melanoma, rhabdomyosarcoma, Ewing sarcoma, osteosarcoma, B-cell neoplasms, multiple myeloma, B-cell lymphoma, B-cell non-Hodgkin’s lymphoma, Hodgkin’s lymphoma, chronic lymphocytic leukemia (CLL), acute myeloid leukemia (AML), chronic myeloid leukemia (CML), acute lymphocytic leukemia (ALL), myelodysplastic syndromes (MDS), cutaneous T-cell lymphoma, retinoblastoma, stomach cancer, urothelial carcinoma, lung cancer, renal cell carcinoma, gastric and esophageal cancer, pancreatic cancer, prostate cancer, breast cancer, colorec
  • the subject can be a subject identified or diagnosed as having an age-related disease or having chronic inflammation.
  • methods of treating cancer in a subject including administering to the subject a therapeutically effective amount of any one of the proteins described herein.
  • methods of treating an infectious disease in a subject including administering to the subject a therapeutically effective amount of any one of the proteins described herein.
  • methods of treating an infectious disease in a subject including administering to the subject a therapeutically effective amount of any one of the proteins described herein or any one of the pharmaceutical compositions described herein.
  • Non-limiting examples of infectious disease include: anthrax, arboviral disease, babesiosis, botulism, brucellosis, campylobacteriosis, cholera, congenital syphilis, covid- 19, dengue virus infections, diphtheria, ehrlichiosis and anaplasmosis, gonorrhea, Hansen’s disease, hantavirus infection, hepatitis, HIV infection, invasive pneumococcal disease, legionellosis, listeriosis, lyme disease, malaria, measles, meningococcal disease, pertussis, rubella, salmonellosis, smallpox, tetanus, tuberculosis, viral hemorrhagic fever, and zika virus disease.
  • these methods can result in a reduction in the number, severity, or frequency of one or more symptoms of the age-related disease in the subject (e.g., as compared to the number, severity, or frequency of the one or more symptoms of the cancer in the subject prior to treatment).
  • the methods can result in a decrease (e.g., about 1% decrease to about 99% decrease, an about 1% decrease to about 95% decrease, about 1% decrease to about 90% decrease, about 1% decrease to about 85% decrease, about 1% decrease to about 80% decrease, about 1% decrease to about 75% decrease, about 1% to about 70% decrease, about 1% decrease to about 65% decrease, about 1% decrease to about 60% decrease, about 1% decrease to about 55% decrease, about 1% decrease to about 50% decrease, about 1% decrease to about 45% decrease, about 1% decrease to about 40% decrease, about 1% decrease to about 35% decrease, about 1% decrease to about 30% decrease, about 1% decrease to about 25% decrease, about 1% decrease to about 20% decrease, about 1% decrease to about 15% decrease, about 1% decrease to about 10% decrease, about 1% decrease to about 5% decrease, about 5% decrease to about 99% decrease, an about 5% decrease to about 95% decrease, about 5% decrease to about 90% decrease, about 5% decrease to about 85% decrease, about 5% decrease to about 80% decrease,
  • the subject or “subject in need of treatment” may be a canine (e.g., a dog), feline (e.g., a cat), equine (e.g., a horse), ovine, bovine, porcine, caprine, primate, e.g., a simian (e.g., a monkey (e.g., marmoset, baboon), or an ape (e.g., a gorilla, chimpanzee, orangutan, or gibbon) or a human; or rodent (e.g., a mouse, a guinea pig, a hamster, or a rat).
  • a canine e.g., a dog
  • feline e.g., a cat
  • equine e.g., a horse
  • ovine, bovine, porcine caprine
  • primate e.g., a simian (e.g.,
  • the subject or “subject in need of treatment” may be a non-human mammal, especially mammals that are conventionally used as models for demonstrating therapeutic efficacy in humans (e.g., murine, lapine, porcine, canine or primate animals) may be employed.
  • Treg Cells In some embodiments, a Treg cell can be administered to the subject. In some embodiments, a Treg cell administered to the subject can be an autologous Treg cell, haploidentical Treg cell, or allogenic Treg cell isolated from peripheral blood or umbilical cord blood.
  • the methods described herein can further include isolating a Treg cell from a subject, culturing the isolated Treg cell in a liquid culture medium, and administering the Treg cell back to the subject.
  • a Treg cell can be isolated using a commercially available kit (see, e.g., EasySep TM Human CD4 + CD127 low CD25 + Regulatory T Cell Isolation Kit or Dynabeads Regulatory CD4 + CD25 + T Cell Kit).
  • the liquid culture medium can include one or more of a single-chain chimeric polypeptide (e.g., any of the exemplary single-chain chimeric polypeptides described herein, e.g., 2t2 or 3t28).
  • the liquid culture medium can include the use of a bead having on its surface CD3 and CD28, and recombinant IL-2 or 2t2.
  • the Treg cell can comprise a chimeric antigen receptor (e.g., a chimeric antigen receptor that includes an extracellular domain that binds specifically to tissue factor, CD26 (e.g., any of the anti-CD26 antigen-binding domains described herein), or CD36).
  • extracellular domains that can bind to tissue factor, CD26 or CD36 are scFvs.
  • Non-limiting examples of anti-CD36 antibodies are commercially available from Invitrogen, Abcam, GeneTex, Novus Biologicals, Proteintech, and EMD Millipore.
  • Treg Cell activating Agents can be administered to the subject.
  • the Treg cell activating agent can be a single-chain chimeric polypeptide (e.g., any of the exemplary single-chain chimeric polypeptides described herein), an anti-tissue factor antibody (e.g., the anti-tissue factor antibodies described in U.S. Patent No.7,968,094 and U.S.
  • Patent No.8,007,795 a soluble RAGE protein, an anti-CD26 antibody (e.g, any of the anti-CD26 antibodies described herein), or an anti-CD36 antibody.
  • a soluble RAGE protein can have a sequence that is at least 80%, at least 85%, at least 90%, at least 95%, at least 99%, or 100% identical to SEQ ID NO: 104 or SEQ ID NO: 105.
  • NK Cells In some embodiments, a NK cell can be administered to the subject.
  • a NK cell administered to the subject can be an autologous NK cell, haploidentical NK cells, or allogeneic NK cells isolated from peripheral blood, umbilical cord blood, or isolated and differentiated from iPSC.
  • the methods described herein can further include isolating a NK cell from a subject, culturing the isolated NK cell in a liquid culture medium, and administering the NK cell back to the subject.
  • a NK cell can be isolated using a commercially available kit (see, e.g., EasySep TM Human NK Cell Isolation Kit, MojoSort Human NK Cell Isolation Kit, and Novus Biologicals Human NK Cell Isolation Kit).
  • the liquid culture medium can include one or more of a multi-chain chimeric polypeptide (e.g., any of the exemplary multi-chain chimeric polypeptides described herein, e.g., 18t15-12s and/or 7t15-21s).
  • the NK cell can comprise a chimeric antigen receptor (e.g., a chimeric antigen receptor that includes an extracellular domain that binds specifically to tissue factor or CD26).
  • extracellular domains that can bind to tissue factor or CD26 are scFvs.
  • Non-limiting examples of an anti-CD26 antibodies are commercially available from Abcam, Invitrogen, and GeneTex.
  • anti-CD26 antibodies are the anti-CD26 antibodies described herein.
  • Non-limiting examples of anti-tissue factor heavy chain variable domain and light chain variable domains are described in U.S. Patent No.7,968,094 and U.S. Patent No.8,007,795.
  • Chimeric antigen receptors include a transmembrane domain, a costimulatory domain (e.g., an intracellular CD28 domain), and a CD3zeta signaling domain.
  • a transmembrane domain can include a sequence that is at least 80%, at least 85%, at least 90%, at least 95%, at least 99%, or 100% identical to SEQ ID NO: 101.
  • a costimulatory domain can include a sequence that is at least 80%, at least 85%, at least 90%, at least 95%, at least 99%, or 100% identical to SEQ ID NO: 102.
  • a CD3zeta signaling domain can include a sequence that is at least 80%, at least 85%, at least 90%, at least 95%, at least 99%, or 100% identical to SEQ ID NO: 103.
  • NK Cell Activating Agents In some embodiments, one or more NK cell activating agents can be administered to the subject.
  • the NK cell activating agent can be one or more multi-chain chimeric polypeptide (e.g., any of the exemplary multi-chain chimeric polypeptides described herein), an anti-tissue factor antibody (e.g., the anti-tissue factor antibodies described in U.S. Patent No.7,968,094 and U.S. Patent No.8,007,795), an anti-CD36 antibody (e.g., the anti-CD36 antibodies commercially available from Invitrogen, Abcam, GeneTex, Novus Biologicals, Proteintech, and EMD Millipore), and an anti-CD26 antibody (e.g., the anti-CD26 antibodies commercially available from Abcam, Invitrogen, and GeneTex).
  • an anti-tissue factor antibody e.g., the anti-tissue factor antibodies described in U.S. Patent No.7,968,094 and U.S. Patent No.8,007,795
  • an anti-CD36 antibody e.g., the anti-CD36 antibodies commercially available
  • NK cell activating agents such as cytokine-based agents, can act by directing activating NK cells or can enhance NK cell activity, such as antibodies mediating antibody-dependent cellular cytotoxicity (ADCC) of NK cells.
  • Multi-Chain Chimeric Polypeptides Provided herein are multi-chain chimeric polypeptides that include (a) a first chimeric polypeptide comprising: (i) a first target-binding domain; (ii) a soluble tissue factor domain; and (iii) a first domain of a pair of affinity domains; (b) a second chimeric polypeptide comprising: (i) a second domain of a pair of affinity domains; and (ii) a second target-binding domain, where the first chimeric polypeptide and the second chimeric polypeptide associate through the binding of the first domain and the second domain of the pair of affinity domains.
  • the first target-binding domain e.g., any of the first target-binding domains described herein
  • the soluble tissue factor domain e.g., any of the exemplary soluble tissue factor domains described herein
  • the first chimeric polypeptide further comprises a linker sequence (e.g., any of the exemplary linker sequences described herein or known in the art) between the first target-binding domain (e.g., any of the exemplary first target-binding domains described herein) and the soluble tissue factor domain (e.g., any of the exemplary soluble tissue factor domains described herein) in the first chimeric polypeptide.
  • a linker sequence e.g., any of the exemplary linker sequences described herein or known in the art
  • the soluble tissue factor domain e.g., any of the exemplary soluble tissue factor domains described herein
  • the first domain of the pair of affinity domains e.g., any of the exemplary first domains of any of the exemplary pairs of affinity domains described herein
  • the first chimeric polypeptide further comprises a linker sequence (e.g., any of the exemplary linker sequences described herein or known in the art) between the soluble tissue factor domain (e.g., any of the exemplary soluble tissue factor domains described herein) and the first domain of the pair of affinity domains (e.g., any of the exemplary first domains of any of the exemplary pairs of affinity domains described herein) in the first chimeric polypeptide.
  • a linker sequence e.g., any of the exemplary linker sequences described herein or known in the art
  • the second domain of the pair of affinity domains e.g., any of the exemplary second domains of any of the exemplary pairs of affinity domains described herein
  • the second target-binding domain e.g., any of the exemplary second target-binding domains described herein
  • the second chimeric polypeptide further comprises a linker sequence (e.g., any of the exemplary linker sequences described herein or known in the art) between the second domain of the pair of affinity domains (e.g., any of the exemplary second domains of any of the exemplary pairs of affinity domains described herein) and the second target- binding domain (e.g., any of the exemplary second target-binding domains described herein) in the second chimeric polypeptide.
  • a linker sequence e.g., any of the exemplary linker sequences described herein or known in the art
  • Tissue Factor Human tissue factor is a 263 amino-acid transmembrane protein containing three domains: (1) a 219-amino acid N-terminal extracellular domain (residues 1-219); (2) a 22-amino acid transmembrane domain (residues 220-242); and (3) a 21-amino acid cytoplasmic C-terminal tail (residues 242-263) ((UniProtKB Identifier Number: P13726).
  • the cytoplasmic tail contains two phosphorylation sites at Ser253 and Ser258, and one S- palmitoylation site at Cys245. Deletion or mutation of the cytoplasmic domain was not found to affect tissue factor coagulation activity.
  • Tissue factor has one S-palmitoylation site in the intracellular domain of the protein at Cys245.
  • the Cys245 is located at the amino acid terminus of the intracellular domain and close to the membrane surface.
  • the tissue factor transmembrane domain is composed of a single-spanning ⁇ -helix.
  • the extracellular domain of tissue factor composed of two fibronectin type III domains, is connected to the transmembrane domain through a six-amino acid linker. This linker provides conformational flexibility to decouple the tissue factor extracellular domain from its transmembrane and cytoplasmic domains.
  • Each tissue factor fibronectin type III module is composed of two overlapping ⁇ sheets with the top sheet domain containing three antiparallel ⁇ -strands and the bottom sheet containing four ⁇ -strands.
  • the ⁇ -strands are connected by ⁇ -loops between strand ⁇ A and ⁇ B, ⁇ C and ⁇ D, and ⁇ E and ⁇ F, all of which are conserved in conformation in the two modules.
  • a unique feature of tissue factor is a 17- amino acid ⁇ -hairpin between strand ⁇ 10 and strand ⁇ 11, which is not a common element of the fibronectin superfamily.
  • the N-terminal domain also contains a 12 amino acid loop between ⁇ 6F and ⁇ 7G that is not present in the C-terminal domain and is unique to tissue factor.
  • a fibronectin type III domain structure is a feature of the immunoglobulin-like family of protein folds and is conserved among a wide variety of extracellular proteins.
  • the zymogen FVII is rapidly converted to FVIIa by limited proteolysis once it binds to tissue to form the active tissue factor-FVIIa complex.
  • the FVIIa which circulates as an enzyme at a concentration of approximately 0.1 nM (1% of plasma FVII), can also bind directly to tissue factor.
  • tissue factor and FVIIa on the tissue factor-FVIIa complex greatly increases the enzymatic activity of FVIIa: an approximate 20- to 100-fold increase in the rate of hydrolysis of small, chromogenic peptidyl substrates, and nearly a million-fold increase in the rate of activation of the natural macromolecular substrates FIX and FX.
  • tissue factor-FVIIa complex on phospholipid bilayer i.e., upon exposure of phosphatidyl-L-serine on membrane surfaces
  • FIX or FX activation increases the rate of FIX or FX activation, in a Ca 2+ -dependent manner, an additional 1,000-fold.
  • the roughly million-fold overall increase in FX activation by tissue factor-FVIIa-phospholipid complex relative to free FVIIa is a critical regulatory point for the coagulation cascade.
  • FVII is a ⁇ 50 kDa, single-chain polypeptide consisting of 406 amino acid residues, with an N-terminal ⁇ -carboxyglutamate-rich (GLA) domain, two epidermal growth factor-like domains (EGF1 and EFG2), and a C-terminal serine protease domain.
  • GLA N-terminal ⁇ -carboxyglutamate-rich
  • EGF1 and EFG2 epidermal growth factor-like domains
  • C-terminal serine protease domain is activated to FVIIa by a specific proteolytic cleavage of the Ile- 154 -Arg 152 bond in the short linker region between the EGF2 and the protease domain. This cleavage results in the light and heavy chains being held together by a single disulfide bond of Cys 135 and Cys 262 .
  • FVIIa binds phospholipid membrane in a Ca 2+ -dependent manner through its N- terminal GLA-domain.
  • GLA domain Immediately C-terminal to the GLA domain is an aromatic stack and two EGF domains.
  • the aromatic stack connects the GLA to EGF1 domain which binds a single Ca 2+ ion. Occupancy of this Ca 2+ -binding site increases FVIIa amidolytic activity and tissue factor association.
  • the catalytic triad consist of His 193 , Asp 242 , and Ser 344 , and binding of a single Ca 2+ ion within the FVIIa protease domain is critical for its catalytic activity.
  • FVIIa Proteolytic activation of FVII to FVIIa frees the newly formed amino terminus at Ile 153 to fold back and be inserted into the activation pocket forming a salt bridge with the carboxylate of Asp 343 to generate the oxyanion hole. Formation of this salt bridge is critical for FVIIa activity. However, oxyanion hole formation does not occur in free FVIIa upon proteolytic activation. As a result, FVIIa circulates in a zymogen-like state that is poorly recognized by plasma protease inhibitors, allowing it to circulate with a half-life of approximately 90 minutes. Tissue factor-mediated positioning of the FVIIa active site above the membrane surface is important for FVIIa towards cognate substrates.
  • Free FVIIa adopts a stable, extended structure when bound to the membrane with its active site positioned ⁇ 80 ⁇ above the membrane surface.
  • the FVa active site Upon FVIIa binding to tissue factor, the FVa active site is repositioned ⁇ 6 ⁇ closer to the membrane. This modulation may aid in a proper alignment of the FVIIa catalytic triad with the target substrate cleavage site.
  • GLA- domainless FVIIa it has been shown that the active site was still positioned a similar distance above the membrane, demonstrating that tissue factor is able to fully support FVIIa active site positioning even in the absence of FVIIa-membrane interaction.
  • tissue factor supported full FVIIa proteolytic activity as long as the tissue factor extracellular domain was tethered in some way to the membrane surface.
  • raising the active site of FVIIa greater than 80 ⁇ above the membrane surface greatly reduced the ability of the tissue factor-FVIIa complex to activate FX but did not diminish tissue factor-FVIIa amidolytic activity.
  • Alanine scanning mutagenesis has been used to assess the role of specific amino acid side chains in the tissue factor extracellular domain for interaction with FVIIa (Gibbs et al., Biochemistry 33(47): 14003-14010, 1994; Schullek et al., J Biol Chem 269(30): 19399-19403, 1994).
  • Thr 60 is only partially solvent-exposed and may play a local structural role rather than making a significant contact with ligand.
  • the binding site extends onto the concave side of the intermodule angle involving Glu 24 and Gln 110 , and potentially the more distant residue Val 207 .
  • the binding region extends from Asp58 onto a convex surface area formed by Lys 48 , Lys 46 , Gln 37 , Asp 44 , and Trp 45 .
  • Trp 45 and Asp 44 do not interact independently with FVIIa, indicating that the mutational effect at the Trp 45 position may reflect a structural importance of this side chain for the local packing of the adjacent Asp 44 and Gln 37 side chain.
  • the interactive area further includes two surface- exposed aromatic residues, Phe 76 and Tyr 78 , which form part of the hydrophobic cluster in the N-module.
  • the known physiologic substrates of tissue factor-FVIIa are FVII, FIX, and FX and certain proteinase-activated receptors.
  • Mutational analysis has identified a number of residues that, when mutated, support full FVIIa amidolytic activity towards small peptidyl substrates but are deficient in their ability to support macromolecular substrate (i.e., FVII, FIX, and FX) activation (Ruf et al., J Biol Chem 267(31): 22206-22210, 1992; Ruf et al., J Biol Chem 267(9): 6375-6381, 1992; Huang et al., J Biol Chem 271(36): 21752-21757, 1996; Kirchhofer et al., Biochemistry 39(25): 7380-7387, 2000).
  • macromolecular substrate i.e., FVII, FIX, and FX
  • tissue factor loop region at residues 159-165, and residues in or adjacent to this flexible loop have been shown to be critical for the proteolytic activity of the tissue factor-FVIIa complex.
  • the residues Lys 165 and Lys 166 have also been demonstrated to be important for substrate recognition and binding.
  • Lys 165 and Lys 166 face away from each other, with Lys 165 pointing towards FVIIa in most tissue factor-FVIIa structures, and Lys 166 pointing into the substrate binding exosite region in the crystal structure. Putative salt bridge formation between Lys 165 of and Gla 35 of FVIIa would support the notion that tissue factor interaction with the GLA domain of FVIIa modulates substrate recognition.
  • the soluble tissue factor domain can be a wildtype tissue factor polypeptide lacking the signal sequence, the transmembrane domain, and the intracellular domain.
  • the soluble tissue factor domain can be a tissue factor mutant, wherein a wildtype tissue factor polypeptide lacking the signal sequence, the transmembrane domain, and the intracellular domain, and has been further modified at selected amino acids.
  • the soluble tissue factor domain can be a soluble human tissue factor domain. In some examples, the soluble tissue factor domain can be a soluble mouse tissue factor domain. In some examples, the soluble tissue factor domain can be a soluble rat tissue factor domain.
  • soluble human tissue factor domains a mouse soluble tissue factor domain, a rat soluble tissue factor domain, and mutant soluble tissue factor domains are shown below.
  • a soluble tissue factor domain can include a sequence that is at least 70% identical, at least 72% identical, at least 74% identical, at least 76% identical, at least 78% identical, at least 80% identical, at least 82% identical, at least 84% identical, at least 86% identical, at least 88% identical, at least 90% identical, at least 92% identical, at least 94% identical, at least 96% identical, at least 98% identical, at least 99% identical, or 100% identical to SEQ ID NO: 120, 122, 123,
  • a soluble tissue factor domain can include a sequence of SEQ ID NO: 120, 122, 123, 124, or 125, with one to twenty amino acids (e.g., 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, or 20) amino acids removed from its N-terminus and/or one to twenty amino acids (e.g., 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, or 20) amino acids removed from its C-terminus.
  • amino acids e.g., 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, or 20
  • the soluble tissue factor domain is not capable of binding to Factor VIIa. In some examples of any of the single- or multi-chain chimeric polypeptides described herein, the soluble tissue factor domain does not convert inactive Factor X into Factor Xa.
  • the single- or multi-chain chimeric polypeptide does not stimulate blood coagulation in a mammal.
  • the soluble tissue factor domain can be a soluble human tissue factor domain.
  • the soluble tissue factor domain can be a soluble mouse tissue factor domain.
  • the soluble tissue factor domain can be a soluble rat tissue factor domain.
  • the soluble tissue factor domain does not include one or more (e.g., two, three, four, five, six, or seven) of: a lysine at an amino acid position that corresponds to amino acid position 20 of mature wildtype human tissue factor protein; an isoleucine at an amino acid position that corresponds to amino acid position 22 of mature wildtype human tissue factor protein; a tryptophan at an amino acid position that corresponds to amino acid position 45 of mature wildtype human tissue factor protein; an aspartic acid at an amino acid position that corresponds to amino acid position 58 of mature wildtype human tissue factor protein; a tyrosine at an amino acid position that corresponds to amino acid position 94 of mature wildtype human tissue factor protein; an arginine at an amino acid position that corresponds to amino acid position 135 of mature wildtype human tissue factor protein; and a phenylalanine at an amino acid position that corresponds to amino acid position 140 of mature wildtype human tissue factor protein.
  • a lysine at an amino acid position that corresponds to amino acid position
  • the mutant soluble tissue factor possesses the amino acid sequence of SEQ ID NO: 122 or SEQ ID NO: 123.
  • the soluble tissue factor domain can be encoded by a nucleic acid including a sequence that is at least 70% identical, at least 72% identical, at least 74% identical, at least 76% identical, at least 78% identical, at least 80% identical, at least 82% identical, at least 84% identical, at least 86% identical, at least 88% identical, at least 90% identical, at least 92% identical, at least 94% identical, at least 96% identical, at least 98% identical, at least 99% identical, or 100% identical to SEQ ID NO: 121.
  • Linker Sequences In some embodiments, the linker sequence can be a flexible linker sequence.
  • linker sequences that can be used are described in Klein et al., Protein Engineering, Design & Selection 27(10):325–330, 2014; Priyanka et al., Protein Sci.22(2):153–167, 2013.
  • the linker sequence is a synthetic linker sequence.
  • the first chimeric polypeptide can include one, two, three, four, five, six, seven, eight, nine, or ten linker sequence(s) (e.g., the same or different linker sequences, e.g., any of the exemplary linker sequences described herein or known in the art).
  • the second chimeric polypeptide can include one, two, three, four, five, six, seven, eight, nine, or ten linker sequence(s) (e.g., the same or different linker sequences, e.g., any of the exemplary linker sequences described herein or known in the art).
  • a linker sequence can have a total length of 1 amino acid to about 100 amino acids, 1 amino acid to about 90 amino acids, 1 amino acid to about 80 amino acids, 1 amino acid to about 70 amino acids, 1 amino acid to about 60 amino acids, 1 amino acid to about 50 amino acids, 1 amino acid to about 45 amino acids, 1 amino acid to about 40 amino acids, 1 amino acid to about 35 amino acids, 1 amino acid to about 30 amino acids, 1 amino acid to about 25 amino acids, 1 amino acid to about 24 amino acids, 1 amino acid to about 22 amino acids, 1 amino acid to about 20 amino acids, 1 amino acid to about 18 amino acids, 1 amino acid to about 16 amino acids, 1 amino acid to about 14 amino acids, 1 amino acid to about 12 amino acids, 1 amino acid to about 10 amino acids, 1 amino acid to about 8 amino acids, 1 amino acid to about 6 amino acids, 1 amino acid to about 4 amino acids, about 2 amino acids to about 100 amino acids, about 2 amino acids to about 90 amino acids, about 2 amino acids to about 80 amino acids, about 2 amino acids to about 70 amino acids,
  • the linker is rich in glycine (Gly or G) residues. In some embodiments, the linker is rich in serine (Ser or S) residues. In some embodiments, the linker is rich in glycine and serine residues. In some embodiments, the linker has one or more glycine-serine residue pairs (GS), e.g., 1, 2, 3, 4, 5, 6, 7, 8, 9, or 10 or more GS pairs. In some embodiments, the linker has one or more Gly-Gly-Gly-Ser (GGGS) sequences, e.g., 1, 2, 3, 4, 5, 6, 7, 8, 9, or 10 or more GGGS sequences.
  • GS glycine-serine residue pairs
  • GGGS Gly-Gly-Gly-Ser
  • the linker has one or more Gly-Gly-Gly-Gly-Ser (GGGGS) sequences, e.g., 1, 2, 3, 4, 5, 6, 7, 8, 9, or 10 or more GGGGS sequences. In some embodiments, the linker has one or more Gly-Gly-Ser-Gly (GGSG) sequences, e.g., 1, 2, 3, 4, 5, 6, 7, 8, 9, or 10 or more GGSG sequences. In some embodiments, the linker sequence can comprise or consist of NO: 126). In some embodiments, the linker sequence can be encoded by a nucleic acid comprising or consisting of: NO: 127).
  • the linker sequence can comprise or consist of: Target-Binding Domains
  • the first target-binding domain, the second target-binding domain, and/or the additional one or more target-binding domains can be an antigen-binding domain (e.g., any of the exemplary antigen-binding domains described herein or known in the art), a soluble interleukin or cytokine protein (e.g., any of the exemplary soluble interleukin proteins or soluble cytokine proteins described herein), and a soluble interleukin or cytokine receptor (e.g., any of the exemplary soluble interleukin receptors or soluble cytokine receptors described herein).
  • an antigen-binding domain e.g., any of the exemplary antigen-binding domains described herein or known in the art
  • a soluble interleukin or cytokine protein e.g., any of the exemplary soluble interleukin proteins or soluble cytokine proteins
  • one or more of the first target-binding domain e.g., any of the exemplary first target binding domains described herein or known in the art
  • the second target-binding domain e.g., any of the exemplary second target binding domains described herein or known in the art
  • the one or more additional target binding domains can each, independently, bind specifically to a target selected from the group of: bind specifically to a target selected from the group consisting of: CD16a, CD28, CD3 (e.g., one or more of CD3 ⁇ , CD3 ⁇ , CD3 ⁇ , CD3 ⁇ , and CD3 ⁇ ), CD33, CD20, CD19, CD22, CD123, IL-1R, IL-1, VEGF, IL-6R, IL-4, IL-10, PDL-1, TIGIT, PD-1, TIM3, CTLA4, MICA, MICB, IL-6, IL-8, TNF
  • the first target-binding domain, the second target-binding domain, and/or the one or more additional target-binding domains can each independent have a total number of amino acids of about 5 amino acids to about 1000 amino acids, about 5 amino acids to about 950 amino acids, about 5 amino acids to about 900 amino acids, about 5 amino acids to about 850 amino acids, about 5 amino acids to about 800 amino acids, about 5 amino acids to about 750 amino acids, about 5 amino acids to about 700 amino acids, about 5 amino acids to about 650 amino acids, about 5 amino acids to about 600 amino acids, about 5 amino acids to about 550 amino acids, about 5 amino acids to about 500 amino acids, about 5 amino acids to about 450 amino acids, about 5 amino acids to about 400 amino acids, about 5 amino acids to about 350 amino acids, about 5 amino acids to about 300 amino acids, about 5 amino acids to about 280 amino acids, about 5 amino acids to about 260 amino acids, about 5 amino acids to about 240 amino acids, about 5 amino acids to about 350 amino acids, about 5 amino acids to about 300 amino acids, about 5
  • any of the target-binding domains described herein can bind to its target with a dissociation equilibrium constant (KD) of less than 1 x 10 -7 M, less than 1 x 10 -8 M, less than 1 x 10 -9 M, less than 1 x 10 -10 M, less than 1 x 10 -11 M, less than 1 x 10 -12 M, or less than 1 x 10 -13 M.
  • KD dissociation equilibrium constant
  • the antigen-binding protein construct provided herein can bind to an identifying antigen with a KD of about 1 x 10 -3 M to about 1 x 10 -5 M, about 1 x 10 -4 M to about 1 x 10 -6 M, about 1 x 10 -5 M to about 1 x 10 -7 M, about 1 x 10 -6 M to about 1 x 10 -8 M, about 1 x 10 -7 M to about 1 x 10 -9 M, about 1 x 10 -8 M to about 1 x 10 -10 M, or about 1 x 10 -9 M to about 1 x 10 -11 M (inclusive).
  • any of the target-binding domains described herein can bind to its target with a K D of between about 1 pM to about 30 nM (e.g., about 1 pM to about 25 nM, about 1 pM to about 20 nM, about 1 pM to about 15 nM, about 1 pM to about 10 nM, about 1 pM to about 5 nM, about 1 pM to about 2 nM, about 1 pM to about 1 nM, about 1 pM to about 950 pM, about 1 pM to about 900 pM, about 1 pM to about 850 pM, about 1 pM to about 800 pM, about 1 pM to about 750 pM, about 1 pM to about 700 pM, about 1 pM to about 650 pM, about 1 pM to about 600 pM, about 1 pM to about 550 pM, about 1 pM to about 500 pM, about 1
  • any of the target-binding domains described herein can bind to its target with a K D of between about 1 nM to about 10 nM (e.g., about 1 nM to about 9 nM, about 1 nM to about 8 nM, about 1 nM to about 7 nM, about 1 nM to about 6 nM, about 1 nM to about 5 nM, about 1 nM to about 4 nM, about 1 nM to about 3 nM, about 1 nM to about 2 nM, about 2 nM to about 10 nM, about 2 nM to about 9 nM, about 2 nM to about 8 nM, about 2 nM to about 7 nM, about 2 nM to about 6 nM, about 2 nM to about 5 nM, about 2 nM to about 4 nM, about 2 nM to about 3 nM, about 3 nM to about 10 nM, about 3 nM to about 10
  • any of the polypeptides described herein e.g., an electrophoretic mobility shift assay, a filter binding assay, surface plasmon resonance, and a biomolecular binding kinetics assay, etc.
  • Antigen-Binding Domains In some embodiments of any of the single- or multi-chain chimeric polypeptides described herein, the first target-binding domain and the second target-binding domain bind specifically to the same antigen. In some embodiments of these single- or multi- chain chimeric polypeptides, the first target-binding domain and the second target- binding domain bind specifically to the same epitope.
  • the first target-binding domain and the second target-binding domain include the same amino acid sequence. In some embodiments of any of the single- or multi-chain chimeric polypeptides described herein, the first target-binding domain and the second target-binding domain bind specifically to different antigens. In some embodiments of any of the single- or multi-chain chimeric polypeptides described herein, one or both of the first target-binding domain and the second target- binding domain is an antigen-binding domain.
  • the first target-binding domain and the second target-binding domain are each antigen-binding domains.
  • the antigen-binding domain includes or is a scFv or a single domain antibody (e.g., a VHH or a VNAR domain).
  • an antigen-binding domain e.g., any of the antigen-binding domains described herein
  • Patent No.9,035,026) CD28 (see, e.g., those described in U.S. Patent No.7,723,482), CD3 (see, e.g., those described in U.S. Patent No.9,226,962), CD33 (see, e.g., those described in U.S. Patent No.8,759,494), CD20 (see, e.g., those described in WO 2014/026054), CD19 (see, e.g., those described in U.S.
  • Patent No.9,701,758 CD22 (see, e.g., those described in WO 2003/104425), CD123 (see, e.g., those described in WO 2014/130635), IL-1R (see, e.g., those described in U.S. Patent No.8,741,604), IL- 1 (see, e.g., those described in WO 2014/095808), VEGF (see, e.g., those described in U.S. Patent No.9,090,684), IL-6R (see, e.g., those described in U.S. Patent No. 7,482,436), IL-4 (see, e.g., those described in U.S. Patent Application Publication No.
  • IL-10 see, e.g., those described in U.S. Patent Application Publication No.2016/0340413
  • PDL-1 see, e.g., those described in Drees et al., Protein Express. Purif.94:60-66, 2014
  • TIGIT see, e.g., those described in U.S. Patent Application Publication No.2017/0198042
  • PD-1 see, e.g., those described in U.S. Patent No. 7,488,802
  • TIM3 see, e.g., those described in U.S.
  • Patent No.8,552,156 CTLA4 (see, e.g., those described in WO 2012/120125), MICA (see, e.g., those described in WO 2016/154585), MICB (see, e.g., those described in U.S. Patent No.8,753,640), IL-6 (see, e.g., those described in Gejima et al., Human Antibodies 11(4):121-129, 2002), IL-8 (see, e.g., those described in U.S. Patent No.6,117,980), TNF ⁇ (see, e.g., those described in Geng et al., Immunol.
  • CD26a see, e.g., those described in WO 2017/189526
  • CD36 see, e.g., those described in U.S. Patent Application Publication No.2015/0259429
  • ULBP2 see, e.g., those described in U.S. Patent No. 9,273,136
  • CD30 see, e.g., those described in Homach et al., Scand. J. Immunol. 48(5):497-501, 1998)
  • CD200 see, e.g., those described in U.S. Patent No.9,085,623
  • IGF-1R see, e.g., those described in U.S. Patent Application Publication No.
  • MUC4AC see, e.g., those described in WO 2012/170470
  • MUC5AC see, e.g., those described in U.S. Patent No.9,238,084
  • Trop-2 see, e.g., those described in WO 2013/068946
  • CMET see, e.g., those described in Edwardraja et al., Biotechnol. Bioeng.106(3):367-375, 2010
  • EGFR see, e.g., those described in Akbari et al., Protein Expr. Purif.127:8-15, 2016
  • HER1 see, e.g., those described in U.S.
  • HER2 see, e.g., those described in Cao et al., Biotechnol. Lett.37(7):1347-1354, 2015
  • HER3 see, e.g., those described in U.S. Patent No.9,505,843
  • PSMA see, e.g., those described in Parker et al., Protein Expr. Purif.89(2):136-145, 2013
  • CEA see, e.g., those described in WO 1995/015341
  • B7H3 see, e.g., those described in U.S.
  • Patent No.9,371,395) EPCAM (see, e.g., those described in WO 2014/159531), BCMA (see, e.g., those described in Smith et al., Mol. Ther.26(6):1447-1456, 2018), P-cadherin (see, e.g., those described in U.S. Patent No. 7,452,537), CEACAM5 (see, e.g., those described in U.S. Patent No.9,617,345), a UL16-binding protein (see, e.g., those described in WO 2017/083612), HLA-DR (see, e.g., Pistillo et al., Exp. Clin.
  • any of the antigen-binding domains present in any of the single- or multi-chain chimeric polypeptides described herein are each independently selected from the group consisting of: a VHH domain, a VNAR domain, and a scFv.
  • any of the antigen-binding domains described herein is a BiTe, a (scFv) 2 , a nanobody, a nanobody- HSA, a DART, a TandAb, a scDiabody, a scDiabody-CH3, scFv-CH-CL-scFv, a HSAbody, scDiabody-HAS, or a tandem-scFv.
  • a VHH domain is a single monomeric variable antibody domain that can be found in camelids.
  • a VNAR domain is a single monomeric variable antibody domain that can be found in cartilaginous fish.
  • Non-limiting aspects of VHH domains and V NAR domains are described in, e.g., Cromie et al., Curr. Top. Med. Chem.15:2543-2557, 2016; De Genst et al., Dev. Comp.
  • each of the antigen-binding domains in the single- or multi-chain chimeric polypeptides described herein are both VHH domains, or at least one antigen-binding domain is a VHH domain. In some embodiments, each of the antigen-binding domains in the single- or multi-chain chimeric polypeptides described herein are both VNAR domains, or at least one antigen-binding domain is a VNAR domain. In some embodiments, each of the antigen-binding domains in the single- or multi-chain chimeric polypeptides described herein are both scFv domains, or at least one antigen-binding domain is a scFv domain.
  • two or more of polypeptides present in the single- or multi-chain chimeric polypeptide can assemble (e.g., non-covalently assemble) to form any of the antigen-binding domains described herein, e.g., an antigen-binding fragment of an antibody (e.g., any of the antigen-binding fragments of an antibody described herein), a VHH-scAb, a VHH-Fab, a Dual scFab, a F(ab’)2, a diabody, a crossMab, a DAF (two- in-one), a DAF (four-in-one), a DutaMab, a DT-IgG, a knobs-in-holes common light chain, a knobs-in-holes assembly, a charge pair, a Fab-arm exchange, a SEEDbody, a LUZ-Y, a Fcab, a ⁇ -body, an orthogonal Fab
  • Non-limiting examples of an antigen-binding fragment of an antibody include an Fv fragment, a Fab fragment, a F(ab') 2 fragment, and a Fab' fragment.
  • an antigen-binding fragment of an antibody is an antigen-binding fragment of an IgG (e.g., an antigen-binding fragment of IgG1, IgG2, IgG3, or IgG4) (e.g., an antigen-binding fragment of a human or humanized IgG, e.g., human or humanized IgG1, IgG2, IgG3, or IgG4); an antigen-binding fragment of an IgA (e.g., an antigen-binding fragment of IgA1 or IgA2) (e.g., an antigen-binding fragment of a human or humanized IgA, e.g., a human or humanized IgA1 or IgA2); an antigen-binding fragment of an IgD (e.g., an antigen-binding fragment of a human or humanized IgD); an antigen-binding fragment of an IgE (e.g., an antigen-binding fragment of a human
  • any of the antigen-binding domains described herein can bind to an antigen selected from the group consisting of: a protein, a carbohydrate, a lipid, and a combination thereof. Additional examples and aspects of antigen-binding domains are known in the art. Soluble Interleukin or Cytokine Protein In some embodiments of any of the single- or multi-chain chimeric polypeptides described herein, one or both of the first target-binding domain and the second target- binding domain can be a soluble interleukin protein or soluble cytokine protein.
  • the soluble interleukin or soluble cytokine protein is selected from the group of: IL-2, IL-3, IL-7, IL-8, IL-10, IL-12, IL-15, IL-17, IL-18, IL-21, PDGF-DD, SCF, and FLT3L.
  • soluble IL-2, IL-3, IL-7, IL-8, IL-10, IL-15, IL-17, IL-18, IL-21, PDGF-DD, SCF, and FLT3L are provided below.
  • Human Soluble IL-2 (SEQ ID NO: 129) Human Soluble IL-3 (SEQ ID NO: 130) a n g Human Soluble IL-7 (SEQ ID NO: 131) Human Soluble IL-8 (SEQ ID NO: 132) Human Soluble IL-10 (SEQ ID NO: 133) Human Soluble IL-15 (SEQ ID NO: 134) Human Soluble IL-17 (SEQ ID NO: 135) Human Soluble IL-18 (SEQ ID NO: 136) Human Soluble PDGF-DD (SEQ ID NO: 137) Human Soluble SCF (SEQ ID NO: 138) Human Soluble FLT3L (SEQ ID NO: 139)
  • soluble MICA, MICB, ULBP1, ULBP2, ULBP3, ULBP4, ULBP5, and ULBP6 are provided below.
  • Human Soluble MICA Human Soluble MICB (SEQ ID NO: 141) Human Soluble ULBP1 (SEQ ID NO: 142) Human Soluble ULBP2 (SEQ ID NO: 143) Human Soluble ULBP3 (SEQ ID NO: 144) Human Soluble ULBP4 (SEQ ID NO: 145) Human Soluble ULBP5 (SEQ ID NO: 146) Human Soluble ULBP6 (SEQ ID NO: 147) Additional examples of soluble interleukin proteins and soluble cytokine proteins are known in the art.
  • Soluble Receptor In some embodiments of any of the single- or multi-chain chimeric polypeptides described herein, one or both of the first target-binding domain and the second target- binding domain is a soluble interleukin receptor, a soluble cytokine receptor or a ligand receptor. In some embodiments, the soluble receptor is a soluble TGF- ⁇ receptor II (TGF- ⁇ RII) (see, e.g., those described in Yung et al., Am. J. Resp. Crit. Care Med.
  • TGF- ⁇ RII soluble TGF- ⁇ receptor II
  • a soluble TGF- ⁇ RIII see, e.g., those described in Heng et al., Placenta 57:320, 2017
  • a soluble NKG2D see, e.g., Cosman et al., Immunity 14(2):123- 133, 2001; Costa et al., Front. Immunol., Vol.9, Article 1150, May 29, 2018; doi: 10.3389/fimmu.2018.01150
  • a soluble NKp30 see, e.g., Costa et al., Front.
  • a soluble NKp44 see, e.g., those described in Costa et al., Front. Immunol., Vol.9, Article 1150, May 29, 2018; doi: 10.3389/fimmu.2018.01150
  • a soluble NKp46 see, e.g., Mandelboim et al., Nature 409:1055-1060, 2001; Costa et al., Front.
  • the first chimeric polypeptide further includes one or more (e.g., two, three, four, five, six, seven, eight, nine, or ten) additional target-binding domain(s) (e.g., any of the exemplary target-binding domains described herein or known in the art).
  • At least one of the one or more additional antigen-binding domain(s) can be positioned between the soluble tissue factor domain (e.g., any of the exemplary soluble tissue factor domains described herein or known in the art) and the first domain of the pair of affinity domains (e.g., any of the exemplary first domains of any of the exemplary pairs of affinity domains described herein).
  • the first chimeric polypeptide can further include a linker sequence (e.g., any of the exemplary linker sequences described herein or known in the art) between the soluble tissue factor domain (e.g., any of the exemplary soluble tissue factor domains described herein) and the at least one of the one or more additional target- binding domain(s) (e.g., any of the exemplary target-binding domains described herein or known in the art), and/or a linker sequence (e.g., any of the exemplary linker sequences described herein or known in the art) between the at least one of the one or more additional target-binding domain(s) (e.g., any of the exemplary target-binding domains described herein or known in the art) and the first domain of the pair of affinity domains (e.g., any of the exemplary first domains described herein of any of the exemplary pairs of affinity domains described herein).
  • a linker sequence e.g., any of the exemplary linker sequences
  • the first chimeric polypeptide further includes one or more (e.g., two, three, four, five, six, seven, eight, nine, or ten) additional target-binding domains at the N-terminal and/or C-terminal end of the first chimeric polypeptide.
  • At least one of the one or more additional target-binding domains directly abuts the first domain of the pair of affinity domains (e.g., any of the exemplary first domains described herein of any of the exemplary pairs of affinity domains described herein) in the first chimeric polypeptide.
  • the first chimeric polypeptide further includes a linker sequence (e.g., any of the exemplary linker sequences described herein or known in the art) between the at least one of the one or more additional target-binding domains (e.g., any of the exemplary target-binding domains described herein or known in the art) and the first domain of the pair of affinity domains (e.g., any of the exemplary first domains described herein of any of the exemplary pairs of affinity domains described herein).
  • a linker sequence e.g., any of the exemplary linker sequences described herein or known in the art
  • the at least one of the one or more additional target-binding domains directly abuts the first target-binding domain (e.g., any of the exemplary target-binding domains described herein or known in the art) in the first chimeric polypeptide.
  • the first chimeric polypeptide further comprises a linker sequence (e.g., any of the exemplary linker sequences described herein or known in the art) between the at least one of the one or more additional target-binding domains (e.g., any of the exemplary target-binding domains described herein or known in the art) and the first target-binding domain (e.g., any of the exemplary target-binding domains described herein or known in the art).
  • a linker sequence e.g., any of the exemplary linker sequences described herein or known in the art
  • At least one of the one or more additional target-binding domains is disposed at the N- and/or C-terminus of the first chimeric polypeptide, and at least one of the one or more additional target-binding domains (e.g., any of the exemplary target-binding domains described herein or known in the art) is positioned between the soluble tissue factor domain (e.g., any of the exemplary soluble tissue factor domains described herein or known in the art) and the first domain of the pair of affinity domains (e.g., any of the exemplary first domains of any of the exemplary pairs of affinity domains described herein) in the first chimeric polypeptide.
  • the soluble tissue factor domain e.g., any of the exemplary soluble tissue factor domains described herein or known in the art
  • affinity domains e.g., any of the exemplary first domains of any of the exemplary pairs of affinity domains described herein
  • the at least one additional target-binding domain (e.g., any of the exemplary target-binding domains described herein or known in the art) of the one or more additional target-binding domains disposed at the N-terminus directly abuts the first target-binding domain (e.g., any of the exemplary target-binding domains described herein or known in the art) or the first domain of the pair of affinity domains (e.g., any of the exemplary first domains described herein of any of the exemplary pairs of affinity domains described herein) in the first chimeric polypeptide.
  • the first chimeric polypeptide further comprises a linker sequence (e.g., any of the linker sequences described herein or known in the art) disposed between the at least one additional target-binding domain (e.g., any of the exemplary target-binding domains described herein or known in the art) and the first target-binding domain (e.g., any of the exemplary target-binding domains described herein or known in the art) or the first domain of the pair of affinity domains (e.g., any of the exemplary first domains described herein of any of the exemplary pairs of affinity domains described herein) in the first chimeric polypeptide.
  • a linker sequence e.g., any of the linker sequences described herein or known in the art
  • the at least one additional target-binding domain (e.g., any of the exemplary target-binding domains described herein or known in the art) of the one or more additional target-binding domains disposed at the C-terminus directly abuts the first target-binding domain (e.g., any of the exemplary target-binding domains described herein or known in the art) or the first domain of the pair of affinity domains (e.g., any of the exemplary first domains of any of the exemplary pairs of affinity domains described herein) in the first chimeric polypeptide.
  • the first chimeric polypeptide further includes a linker sequence (e.g., any of the exemplary linker sequences described herein or known in the art) disposed between the at least one additional target-binding domain (e.g., any of the exemplary target-binding domains described herein or known in the art) and the first target-binding domain (e.g., any of the exemplary target-binding domains described herein or known in the art) or the first domain of the pair of affinity domains (e.g., any of the exemplary first domains described herein of any of the exemplary pairs of affinity domains described herein) in the first chimeric polypeptide.
  • a linker sequence e.g., any of the exemplary linker sequences described herein or known in the art
  • the at least one of the one or more additional target-binding domains positioned between the soluble tissue factor domain (e.g., any of the exemplary soluble tissue factor domains described herein) and the first domain of the pair of affinity domains (e.g., any of the first domains described herein or any of the exemplary pairs of affinity domains described herein), directly abuts the soluble tissue factor domain and/or the first domain of the pair of affinity domains.
  • the first chimeric polypeptide further comprises a linker sequence (e.g., any of the exemplary linker sequences described herein or known in the art) disposed (i) between the soluble tissue factor domain (e.g., any of the exemplary soluble tissue factor domains described herein) and the at least one of the one or more additional target-binding domains (e.g., any of the exemplary target-binding domains described herein or known in the art) positioned between the soluble tissue factor domain (e.g., any of the exemplary soluble tissue factor domains described herein) and the first domain of the pair of affinity domains (e.g., any of the exemplary first domains of any of the exemplary pairs of affinity domains described herein), and/or (ii) between the first domain of the pair of affinity domains and the at least one of the one or more additional target-binding domains positioned between the soluble tissue factor domain and the first domain of the pair of affinity domains.
  • a linker sequence e.g.,
  • the second chimeric polypeptide further includes one or more (e.g., two, three, four, five, six, seven, eight, nine, or ten) additional target-binding domains (e.g., any of the exemplary target-binding domains described herein or known in the art) at the N- terminal end and/or the C-terminal end of the second chimeric polypeptide.
  • additional target-binding domains e.g., any of the exemplary target-binding domains described herein or known in the art
  • At least one of the one or more additional target-binding domains directly abuts the second domain of the pair of affinity domains (e.g., any of the exemplary second domains of any of the exemplary pairs of affinity domains described herein) in the second chimeric polypeptide.
  • the second chimeric polypeptide further includes a linker sequence (e.g., any of the exemplary linker sequences described herein or known in the art) between at least one of the one or more additional target- binding domains (e.g., any of the exemplary target-binding domains described herein or known in the art) and the second domain of the pair of affinity domains (e.g., any of the second domains described herein of any of the exemplary pairs of affinity domains described herein) in the second chimeric polypeptide.
  • a linker sequence e.g., any of the exemplary linker sequences described herein or known in the art
  • At least one of the one or more additional target-binding domains directly abuts the second target- binding domain (e.g., any of the target-binding domains described herein or known in the art) in the second chimeric polypeptide.
  • the second chimeric polypeptide further includes a linker sequence (e.g., any of the exemplary linker sequences described herein or known in the art) between at least one of the one or more additional target-binding domains (e.g., any of the exemplary target binding domains described herein or known in the art) and the second target-binding domain (e.g., any of the exemplary target binding domains described herein or known in the art) in the second chimeric polypeptide.
  • a linker sequence e.g., any of the exemplary linker sequences described herein or known in the art
  • two or more (e.g., three or more, four or more, five or more, six or more, seven or more, eight or more, nine or more, or ten or more) of the first target-binding domain, the second target-binding domain, and the one or more additional target-binding domains bind specifically to the same antigen.
  • two or more (e.g., three or more, four or more, five or more, six or more, seven or more, eight or more, nine or more, or ten or more) of the first target-binding domain, the second target-binding domain, and the one or more additional target-binding domains bind specifically to the same epitope.
  • two or more (e.g., three or more, four or more, five or more, six or more, seven or more, eight or more, nine or more, or ten or more) of the first target-binding domain, the second target-binding domain, and the one or more additional target-binding domains include the same amino acid sequence.
  • the first target-binding domain, the second target-binding domain, and the one or more additional target-binding domains each bind specifically to the same antigen.
  • the first target-binding domain, the second target-binding domain, and the one or more additional target-binding domains each bind specifically to the same epitope.
  • the first target-binding domain, the second target-binding domain, and the one or more additional target-binding domains each include the same amino acid sequence. In some embodiments of any of the multi-chain chimeric polypeptides described herein, the first target-binding domain, the second target-binding domain, and the one or more additional target-binding domains bind specifically to different antigens.
  • one or more (e.g., two or more, three or more, four or more, five or more, six or more, seven or more, eight or more, nine or more, or ten or more) of the first target-binding domain, the second target-binding domain, and the one or more target-binding domains is an antigen- binding domain.
  • the first target-binding domain, the second target-binding domain, and the one or more additional target-binding domains are each an antigen-binding domain (e.g., a scFv or a single-domain antibody).
  • a multi-chain chimeric polypeptide includes: 1) a first chimeric polypeptide that includes a first domain of a pair of affinity domains, and 2) a second chimeric polypeptide that includes a second domain of a pair of affinity domains such that the first chimeric polypeptide and the second chimeric polypeptide associate through the binding of the first domain and the second domain of the pair of affinity domains.
  • the pair of affinity domains is a sushi domain from an alpha chain of human IL-15 receptor (IL15R ⁇ ) and a soluble IL-15.
  • a sushi domain also known as a short consensus repeat or type 1 glycoprotein motif, is a common motif in protein-protein interaction.
  • Sushi domains have been identified on a number of protein- binding molecules, including complement components C1r, C1s, factor H, and C2m, as well as the nonimmunologic molecules factor XIII and ⁇ 2-glycoprotein.
  • a typical Sushi domain has approximately 60 amino acid residues and contains four cysteines (Ranganathan, Pac. Symp Biocomput.2000:155-67). The first cysteine can form a disulfide bond with the third cysteine, and the second cysteine can form a disulfide bridge with the fourth cysteine.
  • the soluble IL15 has a D8N or D8A amino acid substitution.
  • the human IL15R ⁇ is a mature full- length IL15R ⁇ .
  • the pair of affinity domains is barnase and barnstar.
  • the pair of affinity domains is a PKA and an AKAP.
  • the pair of affinity domains is an adapter/docking tag module based on mutated RNase I fragments (Rossi, Proc Natl Acad Sci USA.103:6841-6846, 2006; Sharkey et al., Cancer Res.68:5282-5290, 2008; Rossi et al., Trends Pharmacol Sci.
  • a first chimeric polypeptide of a multi-chain chimeric polypeptide includes a first domain of a pair of affinity domains and a second chimeric polypeptide of the multi-chain chimeric polypeptide includes a second domain of a pair of affinity domains, wherein the first domain of the pair of affinity domains and the second domain of the pair of affinity domains bind to each other with a dissociation equilibrium constant (KD) of less than 1 x 10 -7 M, less than 1 x 10 -8 M, less than 1 x 10 -9 M, less than 1 x 10 -10 M, less than 1 x 10 -11 M, less than 1 x 10 -12 M, or less than 1 x 10 -13 M.
  • KD dissociation equilibrium constant
  • the first domain of the pair of affinity domains and the second domain of the pair of affinity domains bind to each other with a KD of about 1 x 10 -4 M to about 1 x 10 -6 M, about 1 x 10 -5 M to about 1 x 10 -7 M, about 1 x 10 -6 M to about 1 x 10 -8 M, about 1 x 10 -7 M to about 1 x 10 -9 M, about 1 x 10 -8 M to about 1 x 10 -10 M, about 1 x 10 -9 M to about 1 x 10 -11 M, about 1 x 10 -10 M to about 1 x 10 -12 M, about 1 x 10 -11 M to about 1 x 10 -13 M, about 1 x 10 -4 M to about 1 x 10 -5 M, about 1 x 10 -5 M to about 1 x 10- 6 M, about 1 x 10 -6 M to about 1 x 10 -7 M, about 1 x 10 -7 M to about 1 x 10 -8 M, about 1 x 10 -4
  • any of a variety of different methods known in the art can be used to determine the KD value of the binding of the first domain of the pair of affinity domains and the second domain of the pair of affinity domains (e.g., an electrophoretic mobility shift assay, a filter binding assay, surface plasmon resonance, and a biomolecular binding kinetics assay, etc.).
  • a first chimeric polypeptide of a multi-chain chimeric polypeptide includes a first domain of a pair of affinity domains and a second chimeric polypeptide of the multi-chain chimeric polypeptide includes a second domain of a pair of affinity domains, wherein the first domain of the pair of affinity domains, the second domain of the pair of affinity domains, or both is about 10 to 100 amino acids in length.
  • a first domain of a pair of affinity domains, a second domain of a pair of affinity domains, or both can be about 10 to 100 amino acids in length, about 15 to 100 amino acids in length, about 20 to 100 amino acids in length, about 25 to 100 amino acids in length, about 30 to 100 amino acids in length, about 35 to 100 amino acids in length, about 40 to 100 amino acids in length, about 45 to 100 amino acids in length, about 50 to 100 amino acids in length, about 55 to 100 amino acids in length, about 60 to 100 amino acids in length, about 65 to 100 amino acids in length, about 70 to 100 amino acids in length, about 75 to 100 amino acids in length, about 80 to 100 amino acids in length, about 85 to 100 amino acids in length, about 90 to 100 amino acids in length, about 95 to 100 amino acids in length, about 10 to 95 amino acids in length, about 10 to 90 amino acids in length, about 10 to 85 amino acids in length, about 10 to 80 amino acids in length, about 10 to 75 amino acids in length, about 10 to 70 amino acids in length, about 10 to 65 amino acids in length
  • a first domain of a pair of affinity domains, a second domain of a pair of affinity domains, or both is about 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95, or 100 amino acids in length.
  • any of the first and/or second domains of a pair of affinity domains disclosed herein can include one or more additional amino acids (e.g., 1, 2, 3, 5, 6, 7, 8, 9, 10, or more amino acids) at its N-terminus and/or C-terminus, so long as the function of the first and/or second domains of a pair of affinity domains remains intact.
  • a sushi domain from an alpha chain of human IL-15 receptor can include one or more additional amino acids at the N-terminus and/or the C-terminus, while still retaining the ability to bind to a soluble IL-15.
  • a soluble IL-15 can include one or more additional amino acids at the N-terminus and/or the C-terminus, while still retaining the ability to bind to a sushi domain from an alpha chain of human IL-15 receptor (IL15R ⁇ ).
  • a non-limiting example of a sushi domain from an alpha chain of IL-15 receptor alpha can include a sequence that is at least 70% identical, at least 75% identical, at least 80% identical, at least 85% identical, at least 90% identical, at least 95% identical, at least 99% identical, or 100% identical to (SEQ ID NO: 148).
  • a sushi domain from an alpha chain of IL15R ⁇ can be encoded by a nucleic acid including
  • a soluble IL-15 can include a sequence that is at least 70% identical, at least 75% identical, at least 80% identical, at least 85% identical, at least 90% identical, at least 95% identical, at least 99% identical, or 100% identical to Q Q S (SEQ ID NO: 134).
  • a soluble IL-15 can be encoded by a nucleic acid including the sequence of Signal Sequence
  • a multi-chain chimeric polypeptide includes a first chimeric polypeptide that includes a signal sequence at its N-terminal end.
  • a multi-chain chimeric polypeptide includes a second chimeric polypeptide that includes a signal sequence at its N-terminal end.
  • both the first chimeric polypeptide of a multi-chain chimeric polypeptide and a second chimeric polypeptide of the multi-chain chimeric polypeptide include a signal sequence.
  • a signal sequence is an amino acid sequence that is present at the N-terminus of a number of endogenously produced proteins that directs the protein to the secretory pathway (e.g., the protein is directed to reside in certain intracellular organelles, to reside in the cell membrane, or to be secreted from the cell).
  • a first chimeric polypeptide of a multi-chain chimeric polypeptide, a second chimeric polypeptide of the multi-chain chimeric polypeptide, or both includes a signal sequence having an amino acid sequence MKWVTFISLLFLFSSAYS (SEQ ID NO: 151).
  • a first chimeric polypeptide of a multi-chain chimeric polypeptide, a second chimeric polypeptide of the multi-chain chimeric polypeptide, or both includes a signal sequence encoded by the nucleic acid sequence: In some embodiments, a first chimeric polypeptide of a multi-chain chimeric polypeptide, a second chimeric polypeptide of the multi-chain chimeric polypeptide, or both includes a signal sequence having an amino acid sequence (SEQ ID NO: 155).
  • a first chimeric polypeptide of a multi-chain chimeric polypeptide, a second chimeric polypeptide of the multi-chain chimeric polypeptide, or both includes a signal sequence having an amino acid sequence (SEQ ID NO: 156).
  • a first chimeric polypeptide of a multi-chain chimeric polypeptide, a second chimeric polypeptide of the multi-chain chimeric polypeptide, or both includes a signal sequence having an amino acid sequence
  • a first chimeric polypeptide of a multi-chain chimeric polypeptide, a second chimeric polypeptide of the multi-chain chimeric polypeptide, or both includes a signal sequence having an amino acid sequence (SEQ ID NO: 158).
  • a first chimeric polypeptide of a multi-chain chimeric polypeptide, a second chimeric polypeptide of the multi-chain chimeric polypeptide, or both includes a signal sequence that is about 10 to 100 amino acids in length.
  • a signal sequence can be about 10 to 100 amino acids in length, about 15 to 100 amino acids in length, about 20 to 100 amino acids in length, about 25 to 100 amino acids in length, about 30 to 100 amino acids in length, about 35 to 100 amino acids in length, about 40 to 100 amino acids in length, about 45 to 100 amino acids in length, about 50 to 100 amino acids in length, about 55 to 100 amino acids in length, about 60 to 100 amino acids in length, about 65 to 100 amino acids in length, about 70 to 100 amino acids in length, about 75 to 100 amino acids in length, about 80 to 100 amino acids in length, about 85 to 100 amino acids in length, about 90 to 100 amino acids in length, about 95 to 100 amino acids in length, about 10 to 95 amino acids in length, about 10 to 90 amino acids in length, about 10 to 85 amino acids in length, about 10 to 80 amino acids in length, about 10 to 75 amino acids in length, about 10 to 70 amino acids in length, about 10 to 65 amino acids in length, about 10 to 60 amino acids in length, about 10 to 55 amino acids in length, about 10 to to 100
  • a signal sequence is about 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95, or 100 amino acids in length.
  • any of the signal sequences disclosed herein can include one or more additional amino acids (e.g., 1, 2, 3, 5, 6, 7, 8, 9, 10, or more amino acids) at its N-terminus and/or C-terminus, so long as the function of the signal sequence remains intact.
  • a signal sequence having the amino acid sequence can include one or more additional amino acids at the N-terminus or C-terminus, while still retaining the ability to direct a first chimeric polypeptide of a multi-chain chimeric polypeptide, a second chimeric polypeptide of the multi-chain chimeric polypeptide, or both to the secretory pathway.
  • a first chimeric polypeptide of a multi-chain chimeric polypeptide, a second chimeric polypeptide of the multi-chain chimeric polypeptide, or both includes a signal sequence that directs the multi-chain chimeric polypeptide into the extracellular space.
  • a multi-chain chimeric polypeptide includes a first chimeric polypeptide that includes a peptide tag (e.g., at the N-terminal end or the C- terminal end of the first chimeric polypeptide).
  • a multi-chain chimeric polypeptide includes a second chimeric polypeptide that includes a peptide tag (e.g., at the N-terminal end or the C-terminal end of the second chimeric polypeptide).
  • both the first chimeric polypeptide of a multi-chain chimeric polypeptide and a second chimeric polypeptide of the multi-chain chimeric polypeptide include a peptide tag.
  • a first chimeric polypeptide of a multi- chain chimeric polypeptide, a second chimeric polypeptide of the multi-chain chimeric polypeptide, or both include two or more peptide tags.
  • Exemplary peptide tags that can be included in a first chimeric polypeptide of a multi-chain chimeric polypeptide, a second chimeric polypeptide of the multi-chain chimeric polypeptide, or both include, without limitation, AviTag (GLNDIFEAQKIEWHE; SEQ ID NO: 159), a calmodulin-tag (KRRWKKNFIAVSAANRFKKISSSGAL; SEQ ID NO: 160), a polyglutamate tag (EEEEEE; SEQ ID NO: 161), an E-tag (GAPVPYPDPLEPR; SEQ ID NO: 162), a FLAG-tag (DYKDDDDK; SEQ ID NO: 163), an HA-tag, a peptide from hemagglutinin (YPYDVPDYA; SEQ ID NO: 164), a his-tag (HHHHH (SEQ ID NO: 165); HHHHHH (SEQ ID NO: 166); HHHHHHH (SEQ ID NO: 167);
  • tissue factor protein is a peptide tag.
  • Peptide tags that can be included in a first chimeric polypeptide of a multi-chain chimeric polypeptide, a second chimeric polypeptide of the multi-chain chimeric polypeptide, or both can be used in any of a variety of applications related to the multi- chain chimeric polypeptide.
  • a peptide tag can be used in the purification of a multi-chain chimeric polypeptide.
  • a first chimeric polypeptide of a multi-chain chimeric polypeptide e.g., a recombinantly expressed first chimeric polypeptide
  • a second chimeric polypeptide of the multi-chain chimeric polypeptide e.g., a recombinantly expressed second chimeric polypeptide
  • both can include a myc tag
  • the multi-chain chimeric polypeptide that includes the myc-tagged first chimeric polypeptide, the myc-tagged second chimeric polypeptide, or both can be purified using an antibody that recognizes the myc tag(s).
  • a first chimeric polypeptide of a multi-chain chimeric polypeptide e.g., a recombinantly expressed first chimeric polypeptide
  • a second chimeric polypeptide of the multi-chain chimeric polypeptide e.g., a recombinantly expressed second chimeric polypeptide
  • both can include a histidine tag
  • the multi-chain chimeric polypeptide that includes the histidine-tagged first chimeric polypeptide, the histidine-tagged second chimeric polypeptide, or both can be purified using a nickel or cobalt chelate.
  • a peptide tag is removed from the first chimeric polypeptide and/or the second chimeric polypeptide of the multi-chain chimeric polypeptide after purification. In some embodiments, a peptide tag is not removed from the first chimeric polypeptide and/or the second chimeric polypeptide of the multi-chain chimeric polypeptide after purification.
  • Peptide tags that can be included in a first chimeric polypeptide of a multi-chain chimeric polypeptide, a second chimeric polypeptide of the multi-chain chimeric polypeptide, or both can be used, for example, in immunoprecipitation of the multi-chain chimeric polypeptide, imaging of the multi-chain chimeric polypeptide (e.g., via Western blotting, ELISA, flow cytometry, and/or immunocytochemistry), and/or solubilization of the multi-chain chimeric polypeptide.
  • a first chimeric polypeptide of a multi-chain chimeric polypeptide, a second chimeric polypeptide of the multi-chain chimeric polypeptide, or both includes a peptide tag that is about 10 to 100 amino acids in length.
  • a peptide tag can be about 10 to 100 amino acids in length, about 15 to 100 amino acids in length, about 20 to 100 amino acids in length, about 25 to 100 amino acids in length, about 30 to 100 amino acids in length, about 35 to 100 amino acids in length, about 40 to 100 amino acids in length, about 45 to 100 amino acids in length, about 50 to 100 amino acids in length, about 55 to 100 amino acids in length, about 60 to 100 amino acids in length, about 65 to 100 amino acids in length, about 70 to 100 amino acids in length, about 75 to 100 amino acids in length, about 80 to 100 amino acids in length, about 85 to 100 amino acids in length, about 90 to 100 amino acids in length, about 95 to 100 amino acids in length, about 10 to 95 amino acids in length, about 10 to 90 amino acids in length, about 10 to 85 amino acids in length, about 10 to 80 amino acids in length, about 10 to 75 amino acids in length, about 10 to 70 amino acids in length, about 10 to 65 amino acids in length, about 10 to 60 amino acids in length, about 10 to 55 amino acids in length, about
  • a peptide tag is about 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95, or 100 amino acids in length.
  • Peptide tags included in a first chimeric polypeptide of a multi-chain chimeric polypeptide, a second chimeric polypeptide of the multi-chain chimeric polypeptide, or both can be of any suitable length.
  • peptide tags can be 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, or more amino acids in length.
  • the two or more peptide tags can be of the same or different lengths.
  • any of the peptide tags disclosed herein may include one or more additional amino acids (e.g., 1, 2, 3, 5, 6, 7, 8, 9, 10, or more amino acids) at the N-terminus and/or C-terminus, so long as the function of the peptide tag remains intact.
  • a myc tag having the amino acid sequence EQKLISEEDL can include one or more additional amino acids (e.g., at the N-terminus and/or the C- terminus of the peptide tag), while still retaining the ability to be bound by an antibody (e.g., 9E10).
  • the first target-binding domain and the second targeting-binding domain each independently bind specifically to a receptor of IL-18 or a receptor of IL-12.
  • the first target-binding domain and the soluble tissue factor domain directly abut each other in the first chimeric polypeptide.
  • the first chimeric polypeptide further comprises a linker sequence (e.g., any of the exemplary linkers described herein) between the first target-binding domain and the soluble tissue factor domain in the first chimeric polypeptide.
  • a linker sequence e.g., any of the exemplary linkers described herein
  • the second domain of the pair of affinity domains and the second target-binding domain directly abut each other in the second chimeric polypeptide.
  • the second chimeric polypeptide further includes a linker sequence (e.g., any of the exemplary linkers described herein) between the second domain of the pair of affinity domains and the second target-binding domain in the second chimeric polypeptide.
  • the soluble tissue factor domain can be any of the exemplary soluble tissue factor domains described herein.
  • the pair of affinity domains can be any of the exemplary pairs of affinity domains described herein.
  • one or both of the first target-binding domain and the second target-binding domain is an agonistic antigen-binding domain.
  • the first target-binding domain and the second target-binding domain are each agonistic antigen-binding domains.
  • the antigen-binding domain includes a scFv or single-domain antibody.
  • one or both of the first target-binding domain and the second target-binding domain is a soluble IL-15 or a soluble IL-18.
  • the first target-binding domain and the second target-binding domain are each independently a soluble IL-15 or a soluble IL-18. In some embodiments of these multi-chain chimeric polypeptides, the first target-binding domain and the second target-binding domain both bind specifically to a receptor of IL-18 or a receptor of IL-12. In some embodiments of these multi-chain chimeric polypeptides, the first target-binding domain and the second target-binding domain bind specifically to the same epitope. In some embodiments of these multi-chain chimeric polypeptides, the first target-binding domain and the second target-binding domain include the same amino acid sequence.
  • the first target- binding domain binds specifically to a receptor for IL-12, and the second target-binding domain binds specifically to a receptor for IL-18. In some embodiments of these multi-chain chimeric polypeptides, the first target-binding domain binds specifically to a receptor for IL-18, and the second target-binding domain bind specifically to a receptor for IL-12. In some embodiments of these multi-chain chimeric polypeptides, the first target- binding domain includes a soluble IL-18 (e.g., a soluble human IL-18).
  • the soluble human IL-18 includes a sequence that is at least 80% identical (e.g., at least 82% identical, at least 84% identical, at least 86% identical, at least 88% identical, at least 90% identical, at least 92% identical, at least 94% identical, at least 96% identical, at least 98% identical, at least 99% identical, or 100% identical) to:
  • the soluble human IL-18 is encoded by a sequence that is at least 80% identical (e.g., at least 82% identical, at least 84% identical, at least 86% identical, at least 88% identical, at least 90% identical, at least 92% identical, at least 94% identical, at least 96% identical, at least 98% identical, at least 99% identical, or 100% identical) to:
  • the second target-binding domain includes a soluble IL-12 (e.g., a soluble IL-12 (e.g., a soluble IL-12 (e.g., a)-2-chain IL-18 (e.g., a soluble IL-12
  • the soluble human IL-15 includes a sequence of soluble human IL-12 ⁇ (p40) and a sequence of soluble human IL- 12 ⁇ (p35).
  • the soluble IL-15 human IL-15 further includes a linker sequence (e.g., any of the exemplary linker sequences described herein) between the sequence of soluble IL-12 ⁇ (p40) and the sequence of soluble human IL-12 ⁇ (p35).
  • the linker sequence comprises GGGGSGGGGSGGGGS (SEQ ID NO: 126).
  • the sequence of soluble human IL-12 ⁇ (p40) comprises a sequence that is at least 80% identical (e.g., at least 82% identical, at least 84% identical, at least 86% identical, at least 88% identical, at least 90% identical, at least 92% identical, at least 94% identical, at least 96% identical, at least 98% identical, at least 99% identical, or 100% identical) to:
  • the soluble human IL-12 ⁇ (p40) is encoded by a sequence that is at least 80% identical (e.g., at least 82% identical, at least 84% identical, at least 86% identical, at least 88% identical, at least 90% identical, at least 92% identical, at least 94% identical, at least 96% identical, at least 98% identical, at least 99% identical, or 100% identical) to:
  • the soluble human IL-12 ⁇ (p35) is encoded by a sequence that is at least 80% identical (e.g., at least 82% identical, at least 84% identical, at least 86% identical, at least 88% identical, at
  • a first chimeric polypeptide is encoded by a sequence that is at least 80% identical (e.g., at least 82% identical, at least 84% identical, at least 86% identical, at least 88% identical, at least 90% identical, at least 92% identical, at least 94% identical, at least 96% identical, at least 98% identical, at least 99% identical, or 100% identical) to:
  • a first chimeric polypeptide can include a sequence that is at least 80% identical (e.g., at least 82% identical, at least 84% identical, at least 86% identical, at least 88% identical, at least 90% identical, at least 92% identical, at least 94% identical, at least 96% identical, at least 98% identical, at least 99% identical, or 100% identical) to:
  • a first chimeric polypeptide is encoded by a sequence that is at least 80% identical (e.g., at least 82% identical, at least 84% identical, at least 86% identical, at least 88% identical, at least 90% identical, at least 92% identical,
  • the second chimeric polypeptide can include a sequence that is at least 80% identical (e.g., at least 82% identical, at least 84% identical, at least 86% identical, at least 88% identical, at least 90% identical, at least 92% identical, at least 94% identical, at least 96% identical, at least 98% identical, at least 99% identical, or 100% identical) to:
  • a second chimeric polypeptide is encoded by a sequence that is at least 80% identical (e.g., at least 82% identical, at least 84% identical, at least 86% identical, at least 88% identical, at least 90% identical, at least 92% identical, at least 94% identical, at least 96% identical, at least 98% identical, at least 99% identical, or 100% identical) to:
  • a second chimeric polypeptide can include a sequence that is at least 80% identical (e.g., at least 82% identical, at least 84% identical, at least 86% identical, at least 88% identical, at least 90% identical, at least 92% identical, at least 94% identical, at least 96% identical, at least 98% identical, at least 99% identical, or 100% identical) to: (S Q NO: 96).
  • a second chimeric polypeptide is encoded by a sequence that is at least 80% identical (e.g., at least 82% identical, at least 84% identical, at least 86% identical, at least 88% identical, at least 90% identical, at least 92% identical, at least 94% identical, at least 96% identical, at least 98% identical, at least 99% identical, or 100% identical) to: Exemplary Multi-Chain Chimeric Polypeptides- Type B
  • the first target-binding domain and the second targeting-binding domain each independently bind specifically to a receptor of IL-7 or a receptor of IL-21.
  • the first target-binding domain and the soluble tissue factor domain directly abut each other in the first chimeric polypeptide.
  • the first chimeric polypeptide further comprises a linker sequence (e.g., any of the exemplary linkers described herein) between the first target-binding domain and the soluble tissue factor domain in the first chimeric polypeptide.
  • the soluble tissue factor domain and the first domain of the pair of affinity domains directly abut each other in the first chimeric polypeptide.
  • the first chimeric polypeptide further includes a linker sequence (e.g., any of the exemplary linkers described herein) between the soluble tissue factor domain and the first domain of the pair of affinity domains in the first chimeric polypeptide.
  • a linker sequence e.g., any of the exemplary linkers described herein
  • the second domain of the pair of affinity domains and the second target-binding domain directly abut each other in the second chimeric polypeptide.
  • the second chimeric polypeptide further includes a linker sequence (e.g., any of the exemplary linkers described herein) between the second domain of the pair of affinity domains and the second target-binding domain in the second chimeric polypeptide.
  • the soluble tissue factor domain can be any of the exemplary soluble tissue factor domains described herein.
  • the pair of affinity domains can be any of the exemplary pairs of affinity domains described herein.
  • one or both of the first target-binding domain and the second target-binding domain is a soluble IL-21 (e.g., a soluble human IL-21 polypeptide) or a soluble IL-7 (e.g., a soluble human IL-7 polypeptide).
  • the first target-binding domain and the second target-binding domain are each independently a soluble IL-21 or a soluble IL-7.
  • the first target-binding domain and the second target-binding domain both bind specifically to a receptor of IL-21 or a receptor of IL-7.
  • the first target-binding domain and the second target-binding domain bind specifically to the same epitope. In some embodiments of these multi-chain chimeric polypeptides, the first target-binding domain and the second target-binding domain include the same amino acid sequence. In some embodiments of these multi-chain chimeric polypeptides, the first target- binding domain binds specifically to a receptor for IL-21, and the second target-binding domain binds specifically to a receptor for IL-7.
  • the first target-binding domain binds specifically to a receptor for IL-7, and the second target-binding domain binds specifically to a receptor for IL-21.
  • the first target- binding domain includes a soluble IL-21 (e.g., a soluble human IL-21).
  • the soluble human IL-21 includes a sequence that is at least 80% identical (e.g., at least 82% identical, at least 84% identical, at least 86% identical, at least 88% identical, at least 90% identical, at least 92% identical, at least 94% identical, at least 96% identical, at least 98% identical, at least 99% identical, or 100% identical) to:
  • the soluble human IL-21 is encoded by a sequence that is at least 80% identical (e.g., at least 82% identical, at least 84% identical, at least 86% identical, at least 88% identical, at least 90% identical, at least 92% identical, at least 94% identical, at least 96% identical, at least 98% identical, at least 99% identical, or 100% identical) to:
  • the soluble human IL-21 is encoded by a sequence that is at least 80% identical (e.g., at least 82% identical, at least 84% identical, at least 86% identical, at least 88% identical, at least 90% identical, at least 92% identical, at least 94% identical, at
  • a first chimeric polypeptide can include a sequence that is at least 80% identical (e.g., at least 82% identical, at least 84% identical, at least 86% identical, at least 88% identical, at least 90% identical, at least 92% identical, at least 94% identical, at least 96% identical, at least 98% identical, at least 99% identical, or 100% identical) to:
  • a first chimeric polypeptide is encoded by a sequence that is at least 80% identical (e.g., at least 82% identical, at least 84% identical, at least 86% identical, at least 88% identical, at least 90% identical, at least 92% identical, at least 94% identical, at least 96% identical, at least 98% identical, at least 99% identical, or 100% identical) to:
  • the second chimeric polypeptide can include a sequence that is at least 80% identical (e.g., at least 82% identical, at least 84% identical, at least 86% identical, at least 88% identical, at least 90% identical
  • the first target-binding domain and the second targeting-binding domain each independently bind specifically to a receptor of IL-7 or a receptor of IL-21.
  • the first target-binding domain and the soluble tissue factor domain directly abut each other in the first chimeric polypeptide.
  • the first chimeric polypeptide further comprises a linker sequence (e.g., any of the exemplary linkers described herein) between the first target-binding domain and the soluble tissue factor domain in the first chimeric polypeptide.
  • a linker sequence e.g., any of the exemplary linkers described herein
  • the soluble tissue factor domain and the first domain of the pair of affinity domains directly abut each other in the first chimeric polypeptide.
  • the first chimeric polypeptide further includes a linker sequence (e.g., any of the exemplary linkers described herein) between the soluble tissue factor domain and the first domain of the pair of affinity domains in the first chimeric polypeptide.
  • a linker sequence e.g., any of the exemplary linkers described herein
  • the second domain of the pair of affinity domains and the second target-binding domain directly abut each other in the second chimeric polypeptide.
  • the second chimeric polypeptide further includes a linker sequence (e.g., any of the exemplary linkers described herein) between the second domain of the pair of affinity domains and the second target-binding domain in the second chimeric polypeptide.
  • the soluble tissue factor domain can be any of the exemplary soluble tissue factor domains described herein.
  • the pair of affinity domains can be any of the exemplary pairs of affinity domains described herein.
  • one or both of the first target-binding domain and the second target-binding domain is a soluble IL-21 (e.g., a soluble human IL-21 polypeptide) or a soluble IL-7 (e.g., a soluble human IL-7 polypeptide).
  • the first target-binding domain and the second target-binding domain are each independently a soluble IL-21 or a soluble IL-7.
  • the first target-binding domain and the second target-binding domain both bind specifically to a receptor of IL-21 or a receptor of IL-7.
  • the first target-binding domain and the second target-binding domain bind specifically to the same epitope. In some embodiments of these multi-chain chimeric polypeptides, the first target-binding domain and the second target-binding domain include the same amino acid sequence. In some embodiments of these multi-chain chimeric polypeptides, the first target- binding domain binds specifically to a receptor for IL-21, and the second target-binding domain binds specifically to a receptor for IL-7.
  • the first target-binding domain binds specifically to a receptor for IL-7
  • the second target-binding domain binds specifically to a receptor for IL-21.
  • the soluble human IL-21 includes a sequence that is at least 80% identical (e.g., at least 82% identical, at least 84% identical, at least 86% identical, at least 88% identical, at least 90% identical, at least 92% identical, at least 94% identical, at least 96% identical, at least 98% identical, at least 99% identical, or 100% identical) to:
  • the soluble human IL-21 is encoded by a sequence that is at least 80% identical (e.g., at least 82% identical, at least 84% identical, at least 86% identical, at least 88% identical, at least 90% identical, at least 92% identical, at least 94% identical, at least 96% identical,
  • a first chimeric polypeptide can include a sequence that is at least 80% identical (e.g., at least 82% identical, at least 84% identical, at least 86% identical, at least 88% identical, at least 90% identical, at least 92% identical, at least 94% identical, at least 96% identical, at least 98% identical, at least 99% identical, or 100% identical) to:
  • a first chimeric polypeptide is encoded by a sequence that is at least 80% identical (e.g., at least 82% identical, at least 84% identical, at least 86% identical, at least 88% identical, at least 90% identical, at least 92% identical, at least 94% identical, at least 96% identical, at least 98% identical, at least 99% identical, or 100% identical) to:
  • the second chimeric polypeptide can include a sequence that is at least 80% identical (e.g., at least 82% identical, at least 84% identical, at least 86% identical, at least 88% identical, at least 90% identical
  • the first target-binding domain and the soluble tissue factor domain directly abut each other in the first chimeric polypeptide.
  • the first chimeric polypeptide further comprises a linker sequence (e.g., any of the exemplary linkers described herein) between the first target-binding domain and the soluble tissue factor domain in the first chimeric polypeptide.
  • the soluble tissue factor domain and the first domain of the pair of affinity domains directly abut each other in the first chimeric polypeptide.
  • the first chimeric polypeptide further includes a linker sequence (e.g., any of the exemplary linkers described herein) between the soluble tissue factor domain and the first domain of the pair of affinity domains in the first chimeric polypeptide.
  • a linker sequence e.g., any of the exemplary linkers described herein
  • the second domain of the pair of affinity domains and the second target-binding domain directly abut each other in the second chimeric polypeptide.
  • the second chimeric polypeptide further includes a linker sequence (e.g., any of the exemplary linkers described herein) between the second domain of the pair of affinity domains and the second target-binding domain in the second chimeric polypeptide.
  • the soluble tissue factor domain can be any of the exemplary soluble tissue factor domains described herein.
  • the pair of affinity domains can be any of the exemplary pairs of affinity domains described herein.
  • the first target- binding domain and the second target-binding domain each independently bind specifically to TGF- ⁇ . In some embodiments of these multi-chain chimeric polypeptides, the first target-binding domain and the second target-binding domain bind specifically to the same epitope. In some embodiments of these multi-chain chimeric polypeptides, the first target-binding domain and the second target-binding domain include the same amino acid sequence.
  • the first target-binding domain and the second target-binding domain is a soluble TGF- ⁇ receptor (e.g., a soluble TGF ⁇ RII receptor, e.g., a soluble human TGF ⁇ RII).
  • the soluble human TGFR ⁇ RII includes a first sequence of soluble human TGFR ⁇ RII and a second sequence of soluble human TGFR ⁇ RII.
  • the soluble human TGFR ⁇ RII includes a linker disposed between the first sequence of soluble human TGFR ⁇ RII and the second sequence of soluble human TGFR ⁇ RII.
  • the linker includes the sequence GGGGSGGGGSGGGGS (SEQ ID NO: 126).
  • the first sequence of soluble human TGFR ⁇ RII receptor comprises a sequence that is at least 80% identical (e.g., at least 82% identical, at least 84% identical, at least 86% identical, at least 88% identical, at least 90% identical, at least 92% identical, at least 94% identical, at least 96% identical, at least 98% identical, at least 99% identical, or 100% identical) to:
  • the second sequence of soluble human TGFR ⁇ RII receptor comprises a sequence that is at least 80% identical (e.g., at least 82% identical, at least 84% identical, at least 86% identical, at least 88% identical, at least 90% identical, at least 92% identical, at least 94% identical, at least 96% identical, at least 98% identical, at least 99% identical, or 100% identical) to: c (SEQ ID NO: 224).
  • the first sequence of soluble human TGFR ⁇ RII receptor is encoded by a sequence that is at least 80% identical (e.g., at least 82% identical, at least 84% identical, at least 86% identical, at least 88% identical, at least 90% identical, at least 92% identical, at least 94% identical, at least 96% identical, at least 98% identical, at least 99% identical, or 100% identical) to:
  • the second sequence of soluble human TGFR ⁇ RII receptor is encoded by a sequence that is at least 80% identical (e.g., at least 82% identical, at least 84% identical, at least 86% identical, at least 88% identical, at least 90% identical, at least 92% identical, at least 94% identical, at least 96% identical, at least 98% identical, at least 99% identical, or 100% identical) to:
  • a first chimeric polypeptide can include a sequence that is at least 80% identical (e.g., at least 82% identical, at least 84% identical, at least 86% identical, at least 88% identical, at least 90% identical, at least 92% identical, at least 94% identical, at least 96% identical, at least 98% identical, at least 99% identical, or 100% identical) to: T K W V
  • a first chimeric polypeptide is encoded by a sequence that is at least 80% identical (e.g., at least 82% identical, at least 84% identical, at least 86% identical, at least 88% identical, at least 90% identical, at least 92% identical, at least 94% identical, at least 96% identical, at least 98% identical, at least 99% identical, or 100% identical) to:
  • the second chimeric polypeptide can include a sequence that is at least 80% identical (e.g., at least 82% identical, at least 84% identical, at least 86% identical, at least 88% identical, at least 99% identical, or 100% identical)
  • the first target-binding domain e.g., any of the exemplary target-binding domains described herein or known in the art
  • the soluble tissue factor domain e.g., any of the exemplary soluble tissue factor domains described herein
  • the single-chain chimeric polypeptide further comprises a linker sequence (e.g., any of the exemplary linker sequences described herein or known in the art) between the first target- binding domain (e.g., any of the exemplary target-binding domains described herein or known in the art) and the soluble tissue factor domain (e.g., any of the exemplary soluble tissue factor domains described herein).
  • a linker sequence e.g., any of the exemplary linker sequences described herein or known in the art
  • the soluble tissue factor domain e.g., any of the exemplary soluble tissue factor domains described herein
  • the second target-binding domain e.g., any of the exemplary target-binding domains described herein or known in the art
  • the single-chain chimeric polypeptide further comprises a linker sequence (e.g., any of the exemplary linker sequences described herein or known in the art) between the soluble tissue factor domain (e.g., any of the exemplary soluble tissue factor domains described herein) and the second target-binding domain (e.g., any of the exemplary target-binding domains described herein or known in the art).
  • a linker sequence e.g., any of the exemplary linker sequences described herein or known in the art
  • the first target-binding domain e.g., any of the exemplary target-binding domains described herein or known in the art
  • the second target-binding domain e.g., any of the exemplary target-binding domains described herein or known in the art
  • the single-chain chimeric polypeptide further comprises a linker sequence (e.g., any of the exemplary linker sequences described herein or known in the art) between the first target-binding domain (e.g., any of the exemplary target-binding domains described herein or known in the art) and the second target-binding domain (e.g., any of the exemplary target-binding domains described herein or known in the art).
  • a linker sequence e.g., any of the exemplary linker sequences described herein or known in the art
  • the second target-binding domain e.g., any of the exemplary target-binding domains described herein or known in the art
  • the soluble tissue factor domain e.g., any of the exemplary soluble tissue factor domains described herein
  • the single-chain chimeric polypeptide further comprises a linker sequence (e.g., any of the exemplary linker sequences described herein or known in the art) between the second target-binding domain (e.g., any of the exemplary target-binding domains described herein or known in the art) and the soluble tissue factor domain (e.g., any of the exemplary soluble tissue factor domains described herein or known in the art).
  • a linker sequence e.g., any of the exemplary linker sequences described herein or known in the art
  • the first target-binding domain and/or the second target-binding domain can independently bind specifically to CD3 (e.g., human CD3) or CD28 (e.g., human CD28).
  • CD3 e.g., human CD3
  • CD28 e.g., human CD28
  • the first target-binding domain binds specifically to CD3 (e.g., human CD3) and the second target-binding domain binds specifically to CD28 (e.g., human CD28).
  • the first target-binding domain binds specifically to CD28 (e.g., human CD28) and the second target-binding domain binds specifically to CD3 (e.g., human CD3).
  • CD28 e.g., human CD28
  • CD3 e.g., human CD3
  • the first target- binding domain and the soluble tissue factor domain directly abut each other.
  • the single-chain chimeric polypeptide further includes a linker sequence (e.g., any of the exemplary linkers described herein) between the first target-binding domain and the soluble tissue factor domain.
  • the soluble tissue factor domain and the second target-binding domain directly abut each other.
  • the single-chain chimeric polypeptide further includes a linker sequence (e.g., any of the exemplary linkers described herein) between the soluble tissue factor domain and the second target-binding domain.
  • one or both of the first target-binding domain and the second target-binding domain is an antigen- binding domain.
  • the first target-binding domain and the second target-binding domain are each an antigen- binding domain (e.g., any of the exemplary antigen-binding domains described herein).
  • the antigen-binding domain includes a scFv or a single domain antibody.
  • an scFv that binds specifically to CD3 can include a sequence that is at least 80% identical (e.g., at least 82% identical, at least 84% identical, at least 86% identical, at least 88% identical, at least 90% identical, at least 92% identical, at least 94% identical, at least 96% identical, at least 98% identical, at least 99% identical, or 100% identical) to:
  • an scFv that binds specifically to CD3 can be encoded by a sequence that is at least 80% identical (e.g., at least 82% identical, at least 84% identical, at least 86% identical, at least 88% identical, at least 90% identical, at least 92% identical, at least 94% identical, at least 96% identical, at least 98% identical, at least 99% identical, or 100% identical) to:
  • an scFv that binds specifically to CD28 can include a sequence that is at least 80% identical (e.g., at least 82% identical, at least 84% identical, at least 86% identical, at least 88% identical, at least 90% identical, at least 92% identical, at least 94% identical, at least 96% identical, at least 98% identical, at least 99% identical, or 100% identical) to:
  • an scFv that binds specifically to CD28 can be encoded by a sequence that is at least 80% identical (e.g., at least 82% identical, at least 84% identical, at least 86% identical, at least 88% identical, at least 90% identical, at least 92% identical, at least 94% identical, at least 96% identical, at least 98% identical, at least 99% identical, or 100% identical) to:
  • the first target- binding domain and/or the second target-binding domain is a soluble receptor (e.g., a soluble CD28 receptor or a soluble CD3 receptor).
  • the soluble tissue factor domain can be any of the exemplary soluble tissue factor domains described herein.
  • a single-chain chimeric polypeptide can include a sequence that is at least 80% identical (e.g., at least 82% identical, at least 84% identical, at least 86% identical, at least 88% identical, at least 90% identical, at least 92% identical, at least 94% identical, at least 96% identical, at least 98% identical, at least 99% identical, or 100% identical) to:
  • a single-chain chimeric polypeptide is encoded by a sequence that is at least 80% identical (e.g., at least 82% identical, at least 84% identical, at least 86% identical, at least 88% identical, at least 90% identical, at least 92% identical, at least 94% identical, at least 96% identical, at least 98% identical, at least 99% identical, or 100% identical) to:
  • a single-chain chimeric polypeptide can include a sequence that is at least 80% identical (e.g., at least 82% identical, at least 84% identical, at least 86% identical, at least 88% identical, at least 90% identical, at least 92% identical, at least 94% identical, at least 96% identical, at least 98% identical, at least 99% identical, or 100% identical) to:
  • a single-chain chimeric polypeptide is encoded by a sequence that is at least 80% identical (e.g., at least 82% identical, at least 84% identical, at least 86% identical, at least 88% identical, at least 90% identical, at least 92% identical, at least 94% identical, at least 96% identical, at least 98% identical, at least 99% identical, or 100% identical) to:
  • the first target-binding domain and/or the second target-binding domain can independently bind specifically to an IL-2 receptor (e.g., human IL-2 receptor).
  • an IL-2 receptor e.g., human IL-2 receptor
  • the first target- binding domain and the soluble tissue factor domain directly abut each other.
  • the single-chain chimeric polypeptide further includes a linker sequence (e.g., any of the exemplary linkers described herein) between the first target-binding domain and the soluble tissue factor domain.
  • the soluble tissue factor domain and the second target-binding domain directly abut each other.
  • the single-chain chimeric polypeptide further includes a linker sequence (e.g., any of the exemplary linkers described herein) between the soluble tissue factor domain and the second target-binding domain.
  • the first target- binding domain and the second target-binding domain is a soluble human IL-2 protein.
  • an IL-2 protein that binds specifically to an IL-2 receptor can include a sequence that is at least 80% identical (e.g., at least 82% identical, at least 84% identical, at least 86% identical, at least 88% identical, at least 90% identical, at least 92% identical, at least 94% identical, at least 96% identical, at least 98% identical, at least 99% identical, or 100% identical) to:
  • an IL-2 protein that binds specifically to an IL-2 receptor can be encoded by a sequence that is at least 80% identical (e.g., at least 82% identical, at least 84% identical, at least 86% identical, at least 88% identical, at least 90% identical, at least 92% identical, at least 94% identical, at least 96% identical, at least 98% identical, at least 99% identical, or 100% identical) to:
  • an IL-2 protein that binds specifically to an IL-2 receptor can be encoded by a sequence that is at least 80% identical (e.g., at least 82% identical, at least 84% identical,
  • a single-chain chimeric polypeptide can include a sequence that is at least 80% identical (e.g., at least 82% identical, at least 84% identical, at least 86% identical, at least 88% identical, at least 90% identical, at least 92% identical, at least 94% identical, at least 96% identical, at least 98% identical, at least 99% identical, or 100% identical) to:
  • a single-chain chimeric polypeptide is encoded by a sequence that is at least 80% identical (e.g., at least 82% identical, at least 84% identical, at least 86% identical, at least 88% identical, at least 90% identical, at least 92% identical, at least 94% identical, at least 96% identical, at least 98% identical, at least 99% identical, or 100% identical) to:
  • a single-chain chimeric polypeptide can include a sequence that is at least 80% identical (e.g., at least 82% identical, at least 84% identical, at least 86% identical, at least 88% identical, at least 90% identical, at least
  • Example 1 Screening of anti-CD26 scFv clones A plate of scFv clones were selected and their binding to CD26, Fc, and proA/L were tested. Controls include binding to Fc (IgG) representing non-specific binding and binding to proA/L (Protein A/L) representing detection of properly folded scFv. For the Fc assays, the scFvs were tested to determine whether they bind specifically to the Fc portion of an antibody.
  • Fc IgG
  • proA/L ProA/L
  • the CD26 binding assays were performed using a CD26-Fc fusion protein, and therefore, the Fc assay was performed to ensure that each scFv does not bind specifically to the Fc portion of an antibody.
  • the proA/L assay is performed to determine whether each scFv has an intact structure with six CDRs and framework regions. The assay utilizes a proA and proL mixture.
  • DNA was also prepared for the scFv constructs and was sent for DNA sequencing to determine light chain (LC)/ heavy chain (HC) region sequences (Figure.1).
  • Example 2. Analysis of DNA sequences of selected scFvs The DNA sequence of each selected clone was translated into an amino acid sequence and the light chain and heavy chain variable domain sequences were determined.
  • the light chain (LC) and heavy chain (HC) amino acid sequences were analyzed to determine unique clone sequences and unique clone numbers. Then, the unique clone sequences were compared with their binding characteristics. As a result, five unique clones with binding were identified (CD26-01D, CD26- 04A, CD26-10B, CD26-12D, and CD26-03B). Sequencing results indicate that the light chain and heavy chain sequences for the five unique clones were intact and the sequences for the CDR-L1, CDR-L2, CDR-L3, CDR-H1, CDR-H2, and CDR-H3 were determined to be unique from each other ( Figure 2).
  • the front portion of the sequence is the light chain (LC) variable domain (underlined), and the terminal portion of the sequence the heavy chain (HC) variable domain (underlined).
  • the LC and HC variable domains are linked to each other with linker sequence, which is shown with place- holding Xs.
  • CD26-03G scFv (SEQ ID NO: 113) CD26-04E scFv (SEQ ID NO: 114) CD26-01F scFv (SEQ ID NO: 115) DIQMTQSPSSLSASVGDRVTITCRASQDVWGYVAWYQQKPGKAPKLLIFSSRSL CD26-01G scFv (SEQ ID NO: 116) CD26-07H scFv amino acid sequence (SEQ ID NO: 117) Example 6.
  • Anti-CD26 IgG1 monoclonal antibodies were constructed based on the scFv sequences provided above in Example 2.
  • the CD26-binding of anti-CD26 monoclonal antibodies was determined with ELISA using either a human CD26-Fc fusion protein or goat anti-human IgG.
  • the CD26-Fc sequences were obtained from the UniProt website and DNA encoding these sequences was synthesized by Genewiz.
  • the construct was made linking the C-terminal of CD26 sequence (N29-P766) with human IgG1 Fc.
  • the nucleic acid and protein sequences of the construct are shown below.
  • the nucleic acid sequence of the CD26-Fc construct (including signal peptide sequence) is as follows (SEQ ID NO: 118): (Signal peptide) ATGAAGTGGGTGACCTTCATCAGCCTGCTGTTCCTGTTCTCCAGCGCCT
  • the amino acid sequence of the human CD26-Fc construct (including signal peptide sequence) is as follows (SEQ ID NO: 119): (Signal peptide) MKWVTFISLLFLFSSAYS
  • the CD26-Fc construct was cloned into a modified retrovirus expression vectors as described previously (Hughes et al., Hum. Gene Ther.16:457–72, 2005), and the expression vectors were transfected into CHO-K1 cells. Expression of the construct in CHO-K1 cells allowed for secretion of the soluble CD26-Fc fusion protein (referred to as CD26-Fc), which can be purified by MabSelect protein A affinity and other chromatography methods. Human CD26-Fc fusion protein (sequence shown above) or goat anti-human IgG was used to coat 96 well Maxisorp plates. The plates were blocked with blocking buffer.
  • Anti-tissue factor antibody (Anti-TF Ab) was used as a negative control and PE-conjugated anti-CD26 (BioLegend) as a positive control. The results demonstrate that CD26Ab-01D and CD26-04A bind to CD26 well and the three tested antibodies have very weak binding (Figure 9).
  • Example 8. ADCC Activities of Anti-CD26 Antibodies ADCC activities of the anti-CD26 monoclonal antibodies were analyzed. Human CD26-transfected CHO cells (CHO26) were labeled with CellTrace Violet and used as target cells, and fresh human NK cells (left: donor-1 and right: donor-2) were used as effector cells.
  • the effector cells were plated with violet-labeled target cells at the indicated effector:target (E:T) ratios with 26Ab-01D or 26Ab-04A at a 5 nM concentration.
  • Anti-tissue factor antibody (Anti-TF Ab) was used as a control.
  • Target cell inhibition (%) was calculated using a formula: (1-viable CHO26 cell number in experimental sample/viable CHO26 cell number in the sample without splenocytes) x 100 on day 2 by flow cytometry.
  • the results show CD26Ab-01D- and CD26Ab-04A- dependent and NK cell-mediated cytotoxicity against CD26 positive CHO cells (Figure 10).
  • the anti-CD26 monoclonal antibodies were probed with SAHRP/ABTS and read using an ELISA plate reader at 405 nM. The results show that ADA was able to block CD26Ab-01D and CD26Ab-04A binding to CD26 molecule ( Figure 11).
  • Example 10 Anti-CD26 CAR Treg cells An anti-human CD26 chimerical antigen receptor (CAR) was generated comprising a HC leader, anti-CD26 scFv, c-myc tag, CD8 ⁇ hinge, CD28 transmembrane/cytoplasmic domain, and CD3 zeta cytoplasmic domain sequences obtained from our own data or the UniProt website and DNA for these sequences was synthesized by Genewiz.
  • CAR CD26 chimerical antigen receptor
  • constructs were made linking the anti-CD26 V L to anti-CD26 VH with a linker to generate a single chain version of anti-CD26 antibody and then directly linking the anti-CD26 scFv sequence to the c-myc tag, CD8 ⁇ hinge, CD28 transmembrane/cytoplasmic domain, CD3 zeta cytoplasmic domain ( Figure 12).
  • the nucleic acid and protein sequences of a construct comprising anti-CD26 CAR are shown below.
  • the nucleic acid sequence of the anti-CD26 CAR construct (including signal peptide sequence) is as follows (SEQ ID NO: 252): (Signal peptide)
  • the amino acid sequence of the anti-CD26 CAR (including signal peptide sequence) is as follows (SEQ ID NO: 253) (CDRs shown in bold): (Signal peptide) MDRLTSSFLLLIVPAYVLS
  • the anti-CD26 CAR construct was cloned into a lentivirus expression vector pLVX-EF1a-IRES-ZsGreen1 (Cat# 631982, Takara).
  • the expression vector was mixed with Lenti-X Packaging Single Shots (Cat# 631275, Takara) and transfected into Lenti-X 293T cells (Cat# 632180, Takara).
  • the lentiviral supernatants from the transfected Lenti- X 293T cells were collected after 3 days incubation at 37 o C in a CO2 incubator.
  • An estimated titer of lentivirus was instantly evaluated with the Lenti-X GoStixTM Plus (Cat# 631280, Takara).
  • the actual lentivirus titers were further evaluated by transduction of Lenti-X 293T cells.
  • Human Treg cells were isolated with a Miltenyi human Treg cell isolation kit (Cat# 130-094-775, Miltenyi) from donor buffy coat PBMCs.
  • the Treg cells were activated with Dynabeads human T-Activator CD3/CD28 (Cat#11131D, ThermoFisher) overnight, and transduced with the lentivirus carrying anti-CD26 CAR at a MOI of 40 measured by flow cytometry.
  • the ⁇ CD26 CAR-transduced Treg cells were verified by stimulation with biotinylated CD26-Fc conjugated Dynabeads M280 Streptavidin (Cat# 11205D, ThermoFisher).
  • ⁇ CD26 CAR Treg cells were activated and expanded using antigen-specific CD26-beads (3-fold) or through the TCR using CD3/CD28 beads (5-fold), but not by non-specific tissue factor conjugated beads or medium only ( Figure 13 and Figure 14).
  • Figure 13 shows images of total Treg cells (upper panels) and anti-CD26 CAR Treg cells (lower panels) stimulated with the specific antigen (CD26/beads), non-specific antigen (TF/beads), or TCR (CD3/CD28/beads) for 3 days, where the ⁇ CD26 CAR Treg cells were shown to be activated and expanded using antigen-specific CD26-beads (3- fold, lower left panel) or through the TCR using CD3/CD28 beads (5-fold, lower right panel), but not by non-specific tissue factor conjugated beads (lower middle panel).
  • CD26/beads specific antigen
  • TF/beads non-specific antigen
  • TCR CD3/CD28/beads
  • the CAR-transduced Treg cells and un-transduced Treg cells were stained with the specific antigen: biotinylated CD26-Fc or a non-specific antigen: biotinylated tissue factor (TF), and detected by R-Phycoerythrin (PE)-conjugated Streptavidin (Cat# 016- 110-084, Jackson ImmunoResearch).
  • specific antigen biotinylated CD26-Fc or a non-specific antigen: biotinylated tissue factor (TF)
  • PE R-Phycoerythrin
  • the ⁇ CD26 CAR Treg cells were specifically stained with CD26-Fc at 100 nM and 10 nM but not with TF, suggesting that anti-CD26 CAR was well displayed on the Treg cell surface and functionally interacts with the specific antigen at an affinity over 10 nM (Figure 15).
  • the ⁇ CD26 CAR-transduced Treg cells and un-transduced Treg cells were stained with the indicated antibodies shown in Figure 16.
  • the ⁇ CD26 CAR Treg cells expressed more CD39 and CTLA-4 compared to the un-transduced Treg cells. The higher CD39 and CTLA-4 expression might be related to a better suppression ability of the ⁇ CD26 CAR Treg cells than the untransduced Treg cells in the suppression assays.
  • ⁇ CD26 CAR Treg cells or untransduced Treg cells were incubated with the CellTrace violet cell proliferation kit (Cat# C34557, ThermoFisher)-labelled Tresp cells from the same donor for 5 days.
  • the suppression of Tresp cell proliferation by ⁇ CD26 CAR Treg cells and untransduced Treg cells were analyzed by flow cytometry.
  • the ⁇ CD26 CAR Treg cells suppressed Tresp proliferation better than the untransduced Treg cells did ( Figure 17).
  • the culture supernatants from the suppression assays were collected for ELISA analysis of the interferon gamma and IL-10 produced by Treg or Tresp cells.

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Abstract

L'invention concerne des protéines comprenant un domaine de liaison à l'antigène anti-CD26. L'invention concerne également des méthodes de traitement d'une maladie liée au vieillissement ou d'une maladie inflammatoire chez un patient qui consistent à administrer au patient une de ces protéines ou une cellule exprimant l'une de ces protéines.
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